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PlusLife Biotech

Full company profile

uuid00037at

Namestring
PlusLife Biotech
Legal namestring
Guangzhou Pluslife Biotechnology Co., Ltd.
Websiteurl
pluslife.com
Company typeenum
Private
Founded yearint
2017
Descriptiontext

PlusLife Biotech (Guangzhou Pluslife Biotechnology Co., Ltd.) is a privately-held molecular diagnostics company founded in 2017 and headquartered in Guangzhou, China, with a regional office in Hong Kong. The company develops point-of-care nucleic acid testing instruments and consumables built on its proprietary RHAM (RNase Hybridization Assisted Amplification) isothermal amplification platform, which delivers PCR-comparable sensitivity without cold-chain logistics or laboratory infrastructure. Its hardware lineup centres on the palm-sized MiniDock device and the eight-channel Dock Pro 8 benchtop instrument, supported by a menu of more than sixteen test cards spanning tuberculosis (MiniDock MTB Test), respiratory infections (SARS-CoV-2, influenza A/B, RSV, Mycoplasma pneumoniae, Strep A), sexually transmitted infections (HPV 16/18/45, TV/MG, GBS), and monkeypox. Manufacturing, R&D, and offices are consolidated in a 10,000+ square-metre Guangzhou facility, with ISO 13485 certification in place since 2021.

The company operates a razor-and-blade revenue model anchored on instrument placement and recurring consumable (test card) sales. Per-test cartridge pricing for the MiniDock MTB Test is approximately USD 3.60 with devices priced near USD 300, positioned as up to 90% cheaper than incumbent molecular platforms. Go-to-market is centred on institutional public-health procurement: the MiniDock MTB Test is the first product endorsed under the World Health Organization's newly established NPOC molecular TB diagnostic category (March 2026) and is the anchor of the Global Fund to Fight AIDS, Tuberculosis and Malaria's 13-country Early Adopter initiative, supported by USD 50 million from the Children's Investment Fund Foundation and additional Stop TB Partnership TB REACH Wave 11 Plus backing. Beyond public-sector TB programmes, PlusLife sells into clinical and outreach settings and operates an adjacent veterinary diagnostics line (PluslifeVet).

Across disclosed funding rounds PlusLife has raised approximately RMB 250 million in equity — a 2021 Series A (RMB 100M led by Qiming Venture Partners), a 2022 Series A+ (RMB 50M led by Qiming Venture Partners), and a 2025 Series B (RMB ~100M led by FC Innovation Venture Fund and Guoju Venture Capital, with Puhua Capital and Qiming Venture Partners) — supplemented by Gates Foundation grant funding for WHO prequalification work and manufacturing capacity. Founder Prof. Sunny Songyang serves as Chief Scientist, and WHO prequalification for the TB test remains in progress with Gates Foundation support.

Short descriptiontext

PlusLife Biotech is a Chinese molecular diagnostics company that builds portable and benchtop isothermal amplification devices (MiniDock, Dock Pro 8) on its proprietary RHAM platform, with a sixteen-plus test-card menu spanning tuberculosis, respiratory infections, STIs, and emerging pathogens, serving primarily national TB programs and global health initiatives in high-burden, resource-limited countries.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
101–250
akta.pro rankint
HeadquartersGuangzhou, China
HQ citystring
Guangzhou
HQ countrystring
China
HQ regionstring
Asia
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
molecular diagnostics, point-of-care testing, isothermal amplification, tuberculosis diagnostics, infectious disease detection
Industry2 codes
1Tuberculosis & Mycobacterial Diseases
CodeHLAKAGAHPrimaryYes
2Microbiology & Infectious Disease Testing (Trial Support)
CodeHLAGAEAFPrimaryNo
NAICS code3 codes
  • In-Vitro Diagnostic Substance Manufacturing325413
  • Analytical Laboratory Instrument Manufacturing334516
  • Navigational, Measuring, Electromedical, and Control Instruments Manufacturing3345
SIC code2 codes
  • In Vitro & In Vivo Diagnostic Substances2835
  • Surgical & Medical Instruments & Apparatus3841
Product category
Molecular Diagnostics (In Vitro Diagnostics)
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model2 records
1Diagnostic Devices and Test Cards
TypeHardware Sales
Description

PlusLife generates revenue through sale of diagnostic instruments (MiniDock, Dock Pro 8) and associated test cards for infectious diseases including TB, respiratory infections, and STIs. Devices provide recurring test card revenue through compatible test menus (16+ tests compatible with Dock Pro 8).

pluslife.com
2MiniDock MTB Test (TB Diagnostic)
TypeOne Time License
Description

Battery-operated near point-of-care TB test priced at $3-4 per test (approximately $3.60 per cartridge). Device costs approximately $300. Tests delivered at decentralized testing settings enabling recurring revenue from national TB programs.

npr.org
Marketing channels3 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels3 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components6 values
Technology or R&D, Supply Chain, Personnel, Operations, Marketing or Sales, Infrastructure
Pricing details1 tier
1MiniDock MTB Test - Per Test Cost
ModelUnit PricingBilling cadencePay-as-you-go
Notes

Test fee approximately $3-4 per test (approximately $3.60 per cartridge). Device costs approximately $300. Priced up to 90% less than current molecular platforms.

npr.org
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

PlusLife Biotech develops and manufactures molecular point-of-care diagnostic devices (MiniDock portable and Dock Pro 8 benchtop) and a menu of single-use test cards built on its proprietary RHAM isothermal nucleic acid amplification technology. The company sells these products primarily to national TB programs, ministries of health, and primary healthcare facilities in high-burden low- and middle-income countries for decentralized infectious disease diagnosis, with tuberculosis as the flagship indication.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 4 values shown
  • 86% sensitivity for sputum samples and 80% for tongue swabs with ~98% specificity for both sample types
+3 more records
Product overview1 text field

Pluslife Biotech offers a molecular point-of-care testing ecosystem centered on RHAM (RNase Hybridization Assisted Amplification) isothermal amplification technology. The portfolio consists of two core diagnostic devices—MiniDock (portable, palm-sized) and Dock Pro 8 (8-channel benchtop system)—complemented by over 16 test cards covering infectious diseases with heavy burdens (including MiniDock MTB Test for tuberculosis), respiratory infections (SARS-CoV-2, Flu A/B, RSV, MP, Strep A), sexually transmitted infections (GBS, HPV 16/18/45, TV/MG), and monkeypox. Supporting accessories include the Pluslife Thermolyse for sample processing and portable power solutions (UPS and solar panels). Software includes mobile apps for Android/iOS and device management software. The platform delivers PCR-comparable performance with extraction-free workflows and no cold-chain requirements, enabling decentralized molecular testing in resource-limited settings.

Product and service18 records
1MiniDock Portable Molecular Diagnostic Device
CategoryDiagnostic Instrument (Hardware)
Description

Palm-sized, lightweight diagnostic device with PCR-comparable accuracy that delivers results in 7–30 minutes with minimal hands-on time. Reagents require no cold-chain transport and the device includes a portable smart charging station, enabling decentralized molecular testing in resource-limited settings.

2Dock Pro 8 Molecular Diagnostic Instrument
CategoryDiagnostic Instrument (Hardware)
Description

Advanced benchtop diagnostic instrument with 8 independently operating test channels for simultaneous testing. Compatible with 16+ test cards and supports LIS system integration, barcode reading, and result printing in a compact stackable design.

3MiniDock MTB Test
CategoryTest Card (Consumable)
Description

Tuberculosis diagnostic test detecting Mycobacterium tuberculosis from sputum or tongue swabs with results in as fast as 5 minutes (up to ~30 minutes). Uses RHAM technology to deliver PCR-level performance without complex lab setup, and dual sample compatibility enables testing for patients unable to expectorate such as children, elderly, and HIV-positive individuals. First WHO-endorsed test in the new NPOC molecular TB diagnostic category.

4SARS-CoV-2/Flu A/Flu B Nucleic Acid Test Card
CategoryTest Card (Consumable)
Description

Multiplex respiratory pathogen test for simultaneous in vitro detection of SARS-CoV-2, Influenza A, and Influenza B RNA from nasal swab samples.

5Flu A/Flu B/RSV Nucleic Acid Test Card
CategoryTest Card (Consumable)
Description

Multiplex respiratory pathogen test for in vitro qualitative detection of Influenza A, Influenza B, and Respiratory Syncytial Virus from nasal, nasopharyngeal, or oropharyngeal swabs.

6Strep A Nucleic Acid Test Card
CategoryTest Card (Consumable)
Description

Rapid nucleic acid test for quick, accurate detection of Group A Streptococcus from oropharyngeal swabs.

7MP (Mycoplasma pneumoniae) Nucleic Acid Test Card
CategoryTest Card (Consumable)
Description

Rapid detection of Mycoplasma pneumoniae P1 adhesion gene from nasal or throat swabs for timely pneumonia diagnosis in children and adolescents.

8RSV Nucleic Acid Test Card
CategoryTest Card (Consumable)
Description

Rapid molecular detection of Respiratory Syncytial Virus from nasal, nasopharyngeal, or oropharyngeal swabs.

9Monkeypox Nucleic Acid Test Card
CategoryTest Card (Consumable)
Description

In vitro qualitative detection of Monkeypox Virus DNA in lesion exudate samples with results in 15–28 minutes.

10HPV 16/18/45 Nucleic Acid Test Card
CategoryTest Card (Consumable)
Description

Rapid detection of high-risk HPV types 16, 18, and 45 DNA in cervical and vulvovaginal swabs for early cancer screening in women in less developed countries (developed in partnership with FIND).

11TV/MG (Trichomonas Vaginalis/Mycoplasma genitalium) Nucleic Acid Test Card
CategoryTest Card (Consumable)
Description

In vitro qualitative detection of Trichomonas Vaginalis and Mycoplasma genitalium DNA from vaginal, cervical, male urethral swabs, and urine.

12GBS (Group B Streptococcus) Nucleic Acid Test Card
CategoryTest Card (Consumable)
Description

Rapid in vitro detection of Group B Streptococcus DNA in vaginal swabs from pregnant women at 35–37 weeks to prevent neonatal complications.

13SARS-CoV-2 Nucleic Acid Test Card
CategoryTest Card (Consumable)
Description

In vitro qualitative detection of SARS-CoV-2 N gene and ORF1ab gene in nasal swabs from suspected COVID-19 cases.

14Pluslife Thermolyse Sample Processing Instrument
CategoryAccessory Instrument (Hardware)
Description

Integrated heating and mixing instrument for uniform liquid sample processing with user-friendly operation and real-time LED displays, used to prepare samples prior to running on the MiniDock or Dock Pro 8 platforms.

15600W Pluslife Portable UPS Power Station
CategoryAccessory Instrument (Hardware)
Description

Portable power station with 576 Wh lithium iron phosphate battery providing AC, USB, USB Type-C, and DC outputs for indoor and outdoor diagnostic deployment, especially in settings without reliable grid electricity.

161200W Pluslife Portable UPS Power Station
CategoryAccessory Instrument (Hardware)
Description

Portable power station with 1152 Wh lithium iron phosphate battery providing stable AC and DC power for compatible electronic equipment in field and decentralized testing settings.

17Portable Solar Panel
CategoryAccessory Instrument (Hardware)
Description

Lightweight, water-resistant folding solar charger with high-efficiency mono-crystalline silicon cells providing USB and DC outputs for off-grid power in remote testing environments.

18Pluslife Software & APP for Human Healthcare
CategorySoftware (Companion Application)
Description

Mobile applications (Pluslife Android and iOS) and device management software (Pluslife PM008, PluslifePad) used to operate Pluslife diagnostic devices, manage diagnostic workflows, and review results for human healthcare.

Scale indicator8 records

Each record includes

Type, Value, Description, Source

Partnership4 partners
Strategic tierStrategicTypeImplementation/ SI/ Consulting PartnerAnnounced on2026-06-23
Description

Aurum Institute implements the 13-country Global Fund Early Adopter initiative on the ground, supporting deployment and implementation of PlusLife MiniDock MTB Test in national TB programs.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-01-01
Description

Stop TB Partnership supports NPOC TB testing scale-up including evidence from PlusLife MiniDock MTB Test informing WHO policy recommendations. TB REACH Wave 11 Plus invests USD 2.7 million across 18 projects in 12 countries to pilot PlusLife testing platform.

3Global Fund to Fight AIDS, Tuberculosis and Malaria
Strategic tierCoreTypeGTM or Marketing PartnerAnnounced on2025-01-01
Description

Global Fund leads Early Adopter initiative deploying PlusLife MiniDock MTB Test across 13 high-burden countries with USD 50 million commitment from CIFF. Products listed for procurement under Global Fund-supported programs.

stoptb.org
4FIND
Strategic tierStrategicTypeStrategic or Co-development PartnerAnnounced on2023-01-01
Description

Collaboration with FIND (Foundation for Innovative New Diagnostics) for HPV project development for the benefit of women in less developed countries. PlusLife HPV 16/18/45 product exhibits excellent clinical performance in FIND partnership.

pluslife.com
Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight7 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

Roche's cobas Liat is a benchtop PCR point-of-care system used for rapid infectious disease testing in clinics and pharmacies; a much broader incumbent offering infectious disease, women's health, and STI menus overlapping with PlusLife's test card portfolio.

TypeBroad incumbent
Description

Abbott's m-PIMA HIV-1 and ID NOW molecular platforms serve global health and POC infectious disease markets; as a global incumbent, Abbott competes via portfolio breadth, established regulatory footprint, and donor relationships in overlapping LMIC procurement.

TypeDirect peer
Description

Qiagen's QIAstat-Dx is a cartridge-based, sample-to-answer molecular diagnostic system used for respiratory and infectious disease testing; comparable in workflow, cartridge-based test menu, and decentralized-care positioning to PlusLife's Dock Pro 8 platform.

TypeBroad incumbent
Description

Hologic's Panther and Aptima molecular systems are widely used for women's health, STI, and infectious disease testing; comparable to PlusLife's HPV and STI test cards on menu and target lab customers, with significantly broader installed base.

TypeDirect peer
Description

Molbio's Truenat MTB is a battery-operated, chip-based molecular TB point-of-care platform widely deployed in primary care settings in LMICs; directly comparable to MiniDock on portability, price, and target customer (national TB programs in high-burden countries).

TypeRegional player
Description

India-based Mylab supplies molecular diagnostic kits and POC platforms for TB, HIV, and infectious diseases; comparable in price-point and target LMIC public health market, but primarily competes in India and South Asia rather than in PlusLife's 13-country Global Fund footprint.

TypeEmerging player
Description

UK-based QuantuMDx is developing the Q-POC portable molecular diagnostic platform for infectious disease and antimicrobial resistance; comparable to MiniDock on portable molecular POC positioning and target global health buyer, though at an earlier commercial stage.

TypeEmerging player
Description

South Korea-based SD Biosensor produces rapid molecular and immunodiagnostic tests (including TB) for global health markets; comparable in approach (cartridge-based, decentralized POC) and donor-channel sales to PlusLife MiniDock.

TypeDirect peer
Description

Cepheid's GeneXpert MTB/RIF is the dominant molecular TB diagnostic platform in high-burden countries; directly competes with PlusLife's MiniDock MTB on the same hospitals, ministries of health, and donor procurement budgets, with a much larger installed base and service network.

TypeEmerging player
Description

South Korea-based Bioneer sells AccuPower molecular diagnostics kits and the ExiStation automated system; overlaps with PlusLife on nucleic acid amplification chemistry and infectious disease menu for global health buyers.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat5 records

Each record includes

Type, Details

Key risks7 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers1 record

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment3 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile2 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

Integration1 record

Each record includes

Title, Type, Description, Source

AI capability2 records

Each record includes

Type, Description, Source

AI maturity
App detail

Has app

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles2 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
Compliance1 record

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds3 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors4 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

PlusLife Biotech

Molecular Diagnostics (In Vitro Diagnostics)pluslife.com

PlusLife Biotech is a Chinese molecular diagnostics company that builds portable and benchtop isothermal amplification devices (MiniDock, Dock Pro 8) on its proprietary RHAM platform, with a sixteen-plus test-card menu spanning tuberculosis, respiratory infections, STIs, and emerging pathogens, serving primarily national TB programs and global health initiatives in high-burden, resource-limited countries.

What PlusLife Biotech does

PlusLife Biotech (Guangzhou Pluslife Biotechnology Co., Ltd.) is a privately-held molecular diagnostics company founded in 2017 and headquartered in Guangzhou, China, with a regional office in Hong Kong. The company develops point-of-care nucleic acid testing instruments and consumables built on its proprietary RHAM (RNase Hybridization Assisted Amplification) isothermal amplification platform, which delivers PCR-comparable sensitivity without cold-chain logistics or laboratory infrastructure. Its hardware lineup centres on the palm-sized MiniDock device and the eight-channel Dock Pro 8 benchtop instrument, supported by a menu of more than sixteen test cards spanning tuberculosis (MiniDock MTB Test), respiratory infections (SARS-CoV-2, influenza A/B, RSV, Mycoplasma pneumoniae, Strep A), sexually transmitted infections (HPV 16/18/45, TV/MG, GBS), and monkeypox. Manufacturing, R&D, and offices are consolidated in a 10,000+ square-metre Guangzhou facility, with ISO 13485 certification in place since 2021.

The company operates a razor-and-blade revenue model anchored on instrument placement and recurring consumable (test card) sales. Per-test cartridge pricing for the MiniDock MTB Test is approximately USD 3.60 with devices priced near USD 300, positioned as up to 90% cheaper than incumbent molecular platforms. Go-to-market is centred on institutional public-health procurement: the MiniDock MTB Test is the first product endorsed under the World Health Organization's newly established NPOC molecular TB diagnostic category (March 2026) and is the anchor of the Global Fund to Fight AIDS, Tuberculosis and Malaria's 13-country Early Adopter initiative, supported by USD 50 million from the Children's Investment Fund Foundation and additional Stop TB Partnership TB REACH Wave 11 Plus backing. Beyond public-sector TB programmes, PlusLife sells into clinical and outreach settings and operates an adjacent veterinary diagnostics line (PluslifeVet).

Across disclosed funding rounds PlusLife has raised approximately RMB 250 million in equity — a 2021 Series A (RMB 100M led by Qiming Venture Partners), a 2022 Series A+ (RMB 50M led by Qiming Venture Partners), and a 2025 Series B (RMB ~100M led by FC Innovation Venture Fund and Guoju Venture Capital, with Puhua Capital and Qiming Venture Partners) — supplemented by Gates Foundation grant funding for WHO prequalification work and manufacturing capacity. Founder Prof. Sunny Songyang serves as Chief Scientist, and WHO prequalification for the TB test remains in progress with Gates Foundation support.

PlusLife Biotech firmographics

Firmographics
Name
PlusLife Biotech
Legal name
Guangzhou Pluslife Biotechnology Co., Ltd.
Website
https://pluslife.com
Company type
Private
Founded year
2017
Operating status
Operating
Headcount range
101–250 employees
Short description
PlusLife Biotech is a Chinese molecular diagnostics company that builds portable and benchtop isothermal amplification devices (MiniDock, Dock Pro 8) on its proprietary RHAM platform, with a sixteen-plus test-card menu spanning tuberculosis, respiratory infections, STIs, and emerging pathogens, serving primarily national TB programs and global health initiatives in high-burden, resource-limited countries.
Ownership category
akta.pro rank

PlusLife Biotech industry classification

Industry
Product category
Molecular Diagnostics (In Vitro Diagnostics)
NAICS
In-Vitro Diagnostic Substance Manufacturing (325413), Analytical Laboratory Instrument Manufacturing (334516), Navigational, Measuring, Electromedical, and Control Instruments Manufacturing (3345)
SIC
In Vitro & In Vivo Diagnostic Substances (2835), Surgical & Medical Instruments & Apparatus (3841)
akta.pro primary industry
Tuberculosis & Mycobacterial Diseases (HLAKAGAH)
akta.pro secondary industry
Microbiology & Infectious Disease Testing (Trial Support) (HLAGAEAF)

Keywords

  • Molecular diagnostics
  • Point-of-care testing
  • Isothermal amplification
  • Tuberculosis diagnostics
  • Infectious disease detection

Where PlusLife Biotech is headquartered

Location

Headquarters

HQ city
Guangzhou
HQ country
China
HQ region
Asia

Offices2 records

Markets served

PlusLife Biotech business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Supply Chain, Personnel, Operations, Marketing or Sales, Infrastructure

Revenue model

  1. Diagnostic Devices and Test Cards: PlusLife generates revenue through sale of diagnostic instruments (MiniDock, Dock Pro 8) and associated test cards for infectious diseases including TB, respiratory infections, and STIs. Devices provide recurring test card revenue through compatible test menus (16+ tests compatible with Dock Pro 8).
  2. MiniDock MTB Test (TB Diagnostic): Battery-operated near point-of-care TB test priced at $3-4 per test (approximately $3.60 per cartridge). Device costs approximately $300. Tests delivered at decentralized testing settings enabling recurring revenue from national TB programs.

Pricing tiers

ModelBillingPrice
Unit PricingPay-as-you-goMiniDock MTB Test - Per Test Cost

Go-to-market motion1 record

Distribution channels3 records

Marketing channels3 records

PlusLife Biotech product offering

Product offering

Core offering

PlusLife Biotech develops and manufactures molecular point-of-care diagnostic devices (MiniDock portable and Dock Pro 8 benchtop) and a menu of single-use test cards built on its proprietary RHAM isothermal nucleic acid amplification technology. The company sells these products primarily to national TB programs, ministries of health, and primary healthcare facilities in high-burden low- and middle-income countries for decentralized infectious disease diagnosis, with tuberculosis as the flagship indication.

Product overview

Pluslife Biotech offers a molecular point-of-care testing ecosystem centered on RHAM (RNase Hybridization Assisted Amplification) isothermal amplification technology. The portfolio consists of two core diagnostic devices—MiniDock (portable, palm-sized) and Dock Pro 8 (8-channel benchtop system)—complemented by over 16 test cards covering infectious diseases with heavy burdens (including MiniDock MTB Test for tuberculosis), respiratory infections (SARS-CoV-2, Flu A/B, RSV, MP, Strep A), sexually transmitted infections (GBS, HPV 16/18/45, TV/MG), and monkeypox. Supporting accessories include the Pluslife Thermolyse for sample processing and portable power solutions (UPS and solar panels). Software includes mobile apps for Android/iOS and device management software. The platform delivers PCR-comparable performance with extraction-free workflows and no cold-chain requirements, enabling decentralized molecular testing in resource-limited settings.

Differentiator

Problem solved

Functional benefit

Products and services

  • MiniDock Portable Molecular Diagnostic Device Palm-sized, lightweight diagnostic device with PCR-comparable accuracy that delivers results in 7–30 minutes with minimal hands-on time. Reagents require no cold-chain transport and the device includes a portable smart charging station, enabling decentralized molecular testing in resource-limited settings.
  • Dock Pro 8 Molecular Diagnostic Instrument Advanced benchtop diagnostic instrument with 8 independently operating test channels for simultaneous testing. Compatible with 16+ test cards and supports LIS system integration, barcode reading, and result printing in a compact stackable design.
  • MiniDock MTB Test Tuberculosis diagnostic test detecting Mycobacterium tuberculosis from sputum or tongue swabs with results in as fast as 5 minutes (up to ~30 minutes). Uses RHAM technology to deliver PCR-level performance without complex lab setup, and dual sample compatibility enables testing for patients unable to expectorate such as children, elderly, and HIV-positive individuals. First WHO-endorsed test in the new NPOC molecular TB diagnostic category.
  • SARS-CoV-2/Flu A/Flu B Nucleic Acid Test Card Multiplex respiratory pathogen test for simultaneous in vitro detection of SARS-CoV-2, Influenza A, and Influenza B RNA from nasal swab samples.
  • Flu A/Flu B/RSV Nucleic Acid Test Card Multiplex respiratory pathogen test for in vitro qualitative detection of Influenza A, Influenza B, and Respiratory Syncytial Virus from nasal, nasopharyngeal, or oropharyngeal swabs.
  • Strep A Nucleic Acid Test Card Rapid nucleic acid test for quick, accurate detection of Group A Streptococcus from oropharyngeal swabs.
  • MP (Mycoplasma pneumoniae) Nucleic Acid Test Card Rapid detection of Mycoplasma pneumoniae P1 adhesion gene from nasal or throat swabs for timely pneumonia diagnosis in children and adolescents.
  • RSV Nucleic Acid Test Card Rapid molecular detection of Respiratory Syncytial Virus from nasal, nasopharyngeal, or oropharyngeal swabs.
  • Monkeypox Nucleic Acid Test Card In vitro qualitative detection of Monkeypox Virus DNA in lesion exudate samples with results in 15–28 minutes.
  • HPV 16/18/45 Nucleic Acid Test Card Rapid detection of high-risk HPV types 16, 18, and 45 DNA in cervical and vulvovaginal swabs for early cancer screening in women in less developed countries (developed in partnership with FIND).
  • TV/MG (Trichomonas Vaginalis/Mycoplasma genitalium) Nucleic Acid Test Card In vitro qualitative detection of Trichomonas Vaginalis and Mycoplasma genitalium DNA from vaginal, cervical, male urethral swabs, and urine.
  • GBS (Group B Streptococcus) Nucleic Acid Test Card Rapid in vitro detection of Group B Streptococcus DNA in vaginal swabs from pregnant women at 35–37 weeks to prevent neonatal complications.
  • SARS-CoV-2 Nucleic Acid Test Card In vitro qualitative detection of SARS-CoV-2 N gene and ORF1ab gene in nasal swabs from suspected COVID-19 cases.
  • Pluslife Thermolyse Sample Processing Instrument Integrated heating and mixing instrument for uniform liquid sample processing with user-friendly operation and real-time LED displays, used to prepare samples prior to running on the MiniDock or Dock Pro 8 platforms.
  • 600W Pluslife Portable UPS Power Station Portable power station with 576 Wh lithium iron phosphate battery providing AC, USB, USB Type-C, and DC outputs for indoor and outdoor diagnostic deployment, especially in settings without reliable grid electricity.
  • 1200W Pluslife Portable UPS Power Station Portable power station with 1152 Wh lithium iron phosphate battery providing stable AC and DC power for compatible electronic equipment in field and decentralized testing settings.
  • Portable Solar Panel Lightweight, water-resistant folding solar charger with high-efficiency mono-crystalline silicon cells providing USB and DC outputs for off-grid power in remote testing environments.
  • Pluslife Software & APP for Human Healthcare Mobile applications (Pluslife Android and iOS) and device management software (Pluslife PM008, PluslifePad) used to operate Pluslife diagnostic devices, manage diagnostic workflows, and review results for human healthcare.

Quantifiable outcome

  • 86% sensitivity for sputum samples and 80% for tongue swabs with ~98% specificity for both sample types
  • +3 more outcomes

Companies that use PlusLife Biotech

Customer profile

Named customers1 record

Segments3 records

Ideal customer profiles2 records

PlusLife Biotech technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Integration1 record

AI capability2 records

Feature3 records

PlusLife Biotech partnerships and signals

Strategic signal

Partnerships

Four partnerships are on record, tiered strategic and core.

  • Aurum InstitutestrategicImplementation/ SI/ Consulting Partner · 23 June 2026Aurum Institute implements the 13-country Global Fund Early Adopter initiative on the ground, supporting deployment and implementation of PlusLife MiniDock MTB Test in national TB programs.
  • Stop TB PartnershipcoreStrategic or Co-development Partner · 1 January 2026Stop TB Partnership supports NPOC TB testing scale-up including evidence from PlusLife MiniDock MTB Test informing WHO policy recommendations. TB REACH Wave 11 Plus invests USD 2.7 million across 18 projects in 12 countries to pilot PlusLife testing platform.
  • Global Fund to Fight AIDS, Tuberculosis and MalariacoreGTM or Marketing Partner · 1 January 2025Global Fund leads Early Adopter initiative deploying PlusLife MiniDock MTB Test across 13 high-burden countries with USD 50 million commitment from CIFF. Products listed for procurement under Global Fund-supported programs.
  • FINDstrategicStrategic or Co-development Partner · 1 January 2023Collaboration with FIND (Foundation for Innovative New Diagnostics) for HPV project development for the benefit of women in less developed countries. PlusLife HPV 16/18/45 product exhibits excellent clinical performance in FIND partnership.

Scale indicators8 records

Recent moves6 records

Expansion highlights7 records

PlusLife Biotech competitors and assessment

Company assessment

Broad incumbents

  • Roche Diagnostics: Roche's cobas Liat is a benchtop PCR point-of-care system used for rapid infectious disease testing in clinics and pharmacies; a much broader incumbent offering infectious disease, women's health, and STI menus overlapping with PlusLife's test card portfolio.
  • Abbott: Abbott's m-PIMA HIV-1 and ID NOW molecular platforms serve global health and POC infectious disease markets; as a global incumbent, Abbott competes via portfolio breadth, established regulatory footprint, and donor relationships in overlapping LMIC procurement.
  • Hologic: Hologic's Panther and Aptima molecular systems are widely used for women's health, STI, and infectious disease testing; comparable to PlusLife's HPV and STI test cards on menu and target lab customers, with significantly broader installed base.

Direct peers

  • Qiagen: Qiagen's QIAstat-Dx is a cartridge-based, sample-to-answer molecular diagnostic system used for respiratory and infectious disease testing; comparable in workflow, cartridge-based test menu, and decentralized-care positioning to PlusLife's Dock Pro 8 platform.
  • Molbio Diagnostics: Molbio's Truenat MTB is a battery-operated, chip-based molecular TB point-of-care platform widely deployed in primary care settings in LMICs; directly comparable to MiniDock on portability, price, and target customer (national TB programs in high-burden countries).
  • Cepheid (Danaher): Cepheid's GeneXpert MTB/RIF is the dominant molecular TB diagnostic platform in high-burden countries; directly competes with PlusLife's MiniDock MTB on the same hospitals, ministries of health, and donor procurement budgets, with a much larger installed base and service network.

Regional players

  • Mylab Discovery Solutions: India-based Mylab supplies molecular diagnostic kits and POC platforms for TB, HIV, and infectious diseases; comparable in price-point and target LMIC public health market, but primarily competes in India and South Asia rather than in PlusLife's 13-country Global Fund footprint.

Emerging players

  • QuantuMDx: UK-based QuantuMDx is developing the Q-POC portable molecular diagnostic platform for infectious disease and antimicrobial resistance; comparable to MiniDock on portable molecular POC positioning and target global health buyer, though at an earlier commercial stage.
  • SD Biosensor: South Korea-based SD Biosensor produces rapid molecular and immunodiagnostic tests (including TB) for global health markets; comparable in approach (cartridge-based, decentralized POC) and donor-channel sales to PlusLife MiniDock.
  • Bioneer: South Korea-based Bioneer sells AccuPower molecular diagnostics kits and the ExiStation automated system; overlaps with PlusLife on nucleic acid amplification chemistry and infectious disease menu for global health buyers.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat5 records

Key risks7 records

Key highlights7 records

Customer concentration

PlusLife Biotech social profiles

Digital presence

PlusLife Biotech compliance and trust

Trust signal

Compliance1 record

PlusLife Biotech financial estimates

Financial estimate

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Valuation estimate

PlusLife Biotech leadership team

Management profile

Number of profiles

Profiles2 records

PlusLife Biotech funding detail

Funding detail

Funding overview

Funding rounds3 records

Investors4 records

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

PlusLife Biotech M&A and investment

M&A and investment

M&A

Investments

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Frequently asked questions about PlusLife Biotech

What does PlusLife Biotech do?

PlusLife Biotech develops and manufactures molecular point-of-care diagnostic devices (MiniDock portable and Dock Pro 8 benchtop) and a menu of single-use test cards built on its proprietary RHAM isothermal nucleic acid amplification technology. The company sells these products primarily to national TB programs, ministries of health, and primary healthcare facilities in high-burden low- and middle-income countries for decentralized infectious disease diagnosis, with tuberculosis as the flagship indication.

Is PlusLife Biotech a public or private company?

PlusLife Biotech is a private company. It is classified as venture growth investor backed and is currently operating.

When was PlusLife Biotech founded?

PlusLife Biotech was founded in 2017. It employs 101 to 250 people.

Where is PlusLife Biotech based?

PlusLife Biotech is headquartered in Guangzhou, China, in the Asia region.

How does PlusLife Biotech make money?

Two revenue lines are on record. Diagnostic Devices and Test Cards are the primary driver. The others are miniDock MTB Test (TB Diagnostic).

Who are PlusLife Biotech's main competitors?

Broad incumbents on record are Roche Diagnostics, Abbott and Hologic. Direct peers are Qiagen, Molbio Diagnostics and Cepheid (Danaher). Mylab Discovery Solutions is listed as a regional player. Emerging players are QuantuMDx, SD Biosensor and Bioneer.

Does PlusLife Biotech have an API?

No public API is recorded for PlusLife Biotech.

What industry is PlusLife Biotech in?

PlusLife Biotech's product category is Molecular Diagnostics (In Vitro Diagnostics). Its primary akta.pro industry code is HLAKAGAH, Tuberculosis & Mycobacterial Diseases, with a secondary code of HLAGAEAF, Microbiology & Infectious Disease Testing (Trial Support). Its NAICS code is 325413 and its SIC code is 2835.

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Live signals
ForbesWhen Access Follows Innovation: Tuberculosis Testing Enters A New EraPluslife Biotech has reduced the price of its MiniDock Ultra molecular tuberculosis test to $2.60, making it the world's most affordable WHO-endorsed molecular diagnostic for TB. More than 15 high-burden countries have begun rolling out this testing technology through initiatives led by the Global Fund and supported by donors like the Gates Foundation, aiming to replace outdated smear microscopy methods.Caixin GlobalGlobal Fund Backs Chinese Test to Speed TB DiagnosisThe Global Fund announced a $13 million procurement of nearly 3 million rapid TB tests from Chinese company Pluslife Biotech. The tests will be rolled out to medical facilities in 13 countries, including Bangladesh, Benin, and Cameroon, to speed TB diagnosis.GenomeWebRollout of 5,000 Near Point-of-Care TB Test Systems in 13 Countries Begins With $50M in FundingWith approximately $50 million in funding from the Children's Investment Fund Foundation, the Global Fund, and other public health organizations, an initial rollout of 5,000 PlusLife MiniDock Ultra instruments and 3 million tuberculosis tests has begun across 13 countries, coordinated by the Aurum Institute. The new near point-of-care TB diagnostic system, endorsed by the World Health Organization in March, can deliver results in 30 minutes using tongue swab samples at a cost of $3.60 per test and $155 per instrument—substantially lower than legacy molecular testing platforms that cost $10,000 to $20,000 per instrument with $8 per test. The rollout aims to address TB diagnosis challenges exacerbated by COVID-19 pandemic disruptions and global aid cuts, with a full-scale expansion expected in the next Global Fund funding cycle (GC8) next year.News-MedicalNon-invasive swab test offers fast, accurate tuberculosis detection worldwideA prospective study published in The New England Journal of Medicine evaluated the MiniDock MTB, a portable tuberculosis diagnostic device developed by Guangzhou Pluslife Biotech, across 1,380 participants in seven high-burden countries between September 2024 and March 2025. The device achieved 86% sensitivity for sputum samples and 80% for tongue swabs with approximately 98% specificity for both, delivering results in 12-25 minutes and earning acceptance from 94% of healthcare workers. The test could enable decentralized TB diagnosis in low-resource settings under the WHO End TB Strategy, though further real-world implementation research and integration with drug-resistance testing remains necessary.School of Public HealthNo sputum needed: Easy-to-use TB test shows accuracy in 7-country analysisA study published in the New England Journal of Medicine found that the MiniDock MTB test, developed by Chinese company Pluslife Biotech, met World Health Organization accuracy and usability standards for tuberculosis detection across outpatient centers in seven high-burden countries. The battery-operated near point-of-care test achieved 85.7% sensitivity and 97.6% specificity on sputum samples, and notably demonstrated 79.6% sensitivity and 99.5% specificity using non-invasive tongue swabs—a critical advantage since 25-40% of TB-evaluated patients cannot produce sputum. The WHO has now recommended the testing platform and tongue swab use to expand diagnostic access, with implementation guidance for national TB programs expected later this year.The Times of IndiaTuberculosis Detection: New molecular tests to change how TB is detected?New molecular diagnostic platforms from India's Molbio Diagnostics and China's Pluslife Biotech are being evaluated for tongue swab tests that could replace sputum-based tuberculosis detection, with WHO recently recommending such near-point-of-care tests for pilot introduction. India accounts for nearly a fourth of the world's TB burden with 187 cases per lakh population in 2024, yet only about 45% of TB centers currently use molecular diagnostics as the upfront test despite their superior accuracy. Hyderabad-based Huwel has partnered with Pluslife while Molbio awaits clearance, and AI-powered portable x-rays from Qure.ai are being deployed for mass screenings in several Indian states as part of the TB elimination effort.PR NewswirePluslife Biotech - A Greater Bay Area Company Launches First Handheld Covid-19 Nucleic Acid TestPluslife Biotech launched the Pluslife Mini Dock, the first handheld point-of-care nucleic acid testing device for COVID-19, designed to provide qPCR-level accuracy with rapid results. The company has deployed initial test kits to Hong Kong hospitals and clinics to address local pandemic prevention challenges and testing capacity constraints.