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Perineologic

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Namestring
Perineologic
Legal namestring
Perineologic
Company typeenum
Private
Founded yearstring
-
Descriptiontext

Perineologic is a privately held medical device company headquartered at 183 N. Centre Street, Cumberland, Maryland, that develops and commercializes the PrecisionPoint Transperineal Access System (PPTAS), the first FDA-cleared device enabling freehand transperineal biopsy of the prostate. Founded in 2014 by practicing urologist Dr. Matthew J. Allaway—who has more than twenty years of clinical experience at Urology Associates in Cumberland and was himself motivated by safety shortcomings in the transrectal biopsy approach—the company spent roughly four years developing the device before receiving FDA clearance. PrecisionPoint uses a patented clamping mechanism compatible with existing BK ultrasound platforms and cylindrical transrectal probes to allow biopsy access through the perineum rather than the rectum, eliminating bowel prep and antibiotic prophylaxis, reducing infection risk to near zero versus the 2–6% rate associated with the transrectal route, and enabling strategic sampling of the anterior prostate where approximately 94% of post-transrectal missed cancers have been documented. The procedure takes 15–20 minutes under local or twilight anesthesia and requires only two skin punctures for comprehensive sampling.

The company’s commercial model is direct enterprise field sales of the FDA-cleared Class II hardware to urology practices, hospitals, and ambulatory surgery centers, complemented by provider training and certification through a documented provider enrollment program and a patient-facing 'Find a PrecisionPoint Provider' locator that pulls demand toward trained sites. As of mid-2022, approximately 500 U.S. urologists had been trained to use the device, with the system in use across 13+ countries and roughly 70% transperineal biopsy penetration reported in the United Kingdom within two years. Perineologic operates with 1–10 employees, has not disclosed institutional funding, and is led by a commercial team drawn from Boston Scientific, Medtronic, Intuitive Surgical, and Smith+Nephew, with ten issued U.S. patents and five pending applications protecting both the current device and a pipeline of potential future products.

Short descriptiontext

Perineologic is a privately held medical device company that developed the FDA-cleared PrecisionPoint Transperineal Access System for freehand transperineal prostate biopsy, selling directly to urology practices and hospitals across 13+ countries.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1–10
akta.pro rankint
HeadquartersCumberland, United States
HQ citystring
Cumberland
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
prostate biopsy devices, transperineal access systems, urology medical devices, FDA-cleared biopsy equipment, freehand prostate biopsy
NAICS code1 code
  • Surgical Appliance and Supplies Manufacturing339113
SIC code2 codes
  • Surgical & Medical Instruments & Apparatus3841
  • Orthopedic, Prosthetic & Surgical Appliances & Supplies3842
Product category
Urology Medical Devices
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model2 records
1PrecisionPoint Device Sales
TypeHardware Sales
Description

Perineologic generates revenue through the sale of its PrecisionPoint Transperineal Access System medical devices to urology practices, hospitals, and healthcare systems. As a Class II medical device requiring FDA clearance, the product is sold directly to trained providers who perform prostate biopsies using the system.

perineologic.com
2Provider Training and Certification
TypeProfessional Services
Description

The company likely generates revenue through training and certification programs for urologists adopting the PrecisionPoint technique, though specific pricing for training services is not publicly disclosed.

perineologic.com
Marketing channels6 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels3 records

Each record includes

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

Cost components5 values
Personnel, Technology or R&D, Operations, Marketing or Sales, Supply Chain
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 record
1PrecisionPoint
Description

The PrecisionPoint Transperineal Access System (PPTAS) - the first FDA cleared device allowing free-handed transperineal biopsy of the prostate. The device enables urologists to perform prostate biopsies through the perineum, avoiding the rectum entirely.

perineologic.com
Core offering1 text field

Perineologic develops, manufactures, and sells the PrecisionPoint Transperineal Access System (PPTAS), an FDA-cleared Class II medical device that enables urologists to perform freehand transperineal prostate biopsies through the perineum rather than the rectum. The system includes a patented clamping mechanism compatible with existing BK ultrasound platforms and cylindrical transducer probes, eliminating the need for bowel prep or antibiotics and reducing infection risk to nearly zero.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 4 values shown
  • 94% of missed cancers after transrectal biopsies were located in the anterior region of the prostate, which PrecisionPoint can specifically target
+3 more records
Product overview1 text field

Perineologic® is an innovative medical device company focused on developing and delivering technology to improve the safety, precision, and efficiency of healthcare options primarily in the field of urology. The company's core product is the PrecisionPoint® Transperineal Access System (PPTAS), which is the first FDA-cleared device enabling free-handed transperineal biopsy of the prostate. This system revolutionizes prostate biopsy methodology by allowing access through the perineum rather than the rectum, eliminating infection risks and enabling more comprehensive cancer detection. The PPTAS works in conjunction with existing ultrasound platforms (specifically BK ultrasound systems) and enables urologists to perform safer, more accurate prostate biopsies under local anesthesia.

Product and service1 record
1PrecisionPoint® Transperineal Access System (PPTAS)
CategoryUrology Medical Devices
Description

FDA-cleared Class II medical device that enables free-handed transperineal biopsy of the prostate through the perineum, avoiding the rectum entirely. The system eliminates the need for bowel prep and antibiotics, reduces infection risk to nearly 0%, and allows comprehensive sampling of all prostate zones including the anterior region. The procedure takes 15-20 minutes and can be performed under local or twilight anesthesia. Designed for urologists performing prostate biopsies.

Scale indicator5 records

Each record includes

Type, Value, Description, Source

Partnership2 partners
Strategic tierCoreTypeTechnology or Integration
Description

Perineologic's PrecisionPoint system is designed to be compatible with BK ultrasound platforms and cylindrical transrectal ultrasound transducer probes (BK #8658 or equivalent). This integration allows urologists to use their existing BK ultrasound equipment with the PrecisionPoint device, reducing adoption barriers for practices already equipped with BK systems.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Dr. Matthew Allaway's urology practice served as the development and testing site for the PrecisionPoint technology. The practice, a 13,000-square-foot modern medical facility including clinical and research space and the Ambulatory Urologic Surgery Center, represents the foundational partnership where the technology was clinically developed over four years of development.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

Major medtech incumbent with a deep Urology/Pelvic Health portfolio including biopsy, ablation, and prostate diagnostics. Comparable because it is the dominant force in urology devices Perineologic sells into, and former Perineologic executives (Brasington, Tanksley, Tourtellot) all came from Boston Scientific roles.

TypeBroad incumbent
Description

Long-established urology device manufacturer offering prostate biopsy needles, access devices, and procedure kits. Comparable because it competes for the same urology practice purchasing budgets and offers overlapping transrectal/transperineal biopsy supplies.

TypeDirect peer
Description

Medical device company with a dedicated prostate health business (NanoKnife, biopsy, and ablation technologies). Comparable because it sells directly to urology practices for prostate biopsy and focal therapy procedures, overlapping Perineologic's call point.

TypeBroad incumbent
Description

Owns BK Medical, whose ultrasound platforms and TRUS transducers are explicitly compatible with PrecisionPoint. Comparable as both a key integration partner and a potential broader competitor if it expands into procedure-specific access devices.

TypeBroad incumbent
Description

Through Invivo, Philips provides MRI/ultrasound fusion-guided prostate biopsy solutions. Comparable as an alternative diagnostic biopsy workflow competing for urology department capital budgets and procedure referrals.

TypeBroad incumbent
Description

Dominant robotic surgery platform (da Vinci) used after prostate cancer diagnosis, often in conjunction with PrecisionPoint biopsies. Comparable because it shares the same urology ecosystem and a former Perineologic SVP previously held a Director, Key Accounts role at Intuitive.

TypeBroad incumbent
Description

Diversified medtech with urology and pelvic health offerings and a strong sales infrastructure into hospitals and ambulatory surgery centers. Comparable as a potential competitor with resources to enter transperineal access and a previous employer of Perineologic's SVP of Sales.

TypeBroad incumbent
Description

Women's health and diagnostics leader that also serves urology through prostate biopsy and related diagnostics. Comparable because it competes for hospital/urology group purchasing decisions and has biopsy device capabilities.

TypeEmerging player
Description

Developer of robotic-assisted prostate biopsy and focal therapy devices (e.g., iSR'obot Mona Lisa). Comparable as a niche emerging competitor in the same transperineal biopsy category that PrecisionPoint addresses.

TypeBroad incumbent
Description

Established urology and continence care company with prostate surgery and biopsy adjacencies. Comparable as a broader urology incumbent targeting the same clinical customers and could expand into transperineal access devices.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers3 records

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 profile3 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

Feature4 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles8 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 rounds

Each record includes

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

Investors

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 →

Perineologic

Urology Medical Devicesperineologic.com

Perineologic is a privately held medical device company that developed the FDA-cleared PrecisionPoint Transperineal Access System for freehand transperineal prostate biopsy, selling directly to urology practices and hospitals across 13+ countries.

What Perineologic does

Perineologic is a privately held medical device company headquartered at 183 N. Centre Street, Cumberland, Maryland, that develops and commercializes the PrecisionPoint Transperineal Access System (PPTAS), the first FDA-cleared device enabling freehand transperineal biopsy of the prostate. Founded in 2014 by practicing urologist Dr. Matthew J. Allaway—who has more than twenty years of clinical experience at Urology Associates in Cumberland and was himself motivated by safety shortcomings in the transrectal biopsy approach—the company spent roughly four years developing the device before receiving FDA clearance. PrecisionPoint uses a patented clamping mechanism compatible with existing BK ultrasound platforms and cylindrical transrectal probes to allow biopsy access through the perineum rather than the rectum, eliminating bowel prep and antibiotic prophylaxis, reducing infection risk to near zero versus the 2–6% rate associated with the transrectal route, and enabling strategic sampling of the anterior prostate where approximately 94% of post-transrectal missed cancers have been documented. The procedure takes 15–20 minutes under local or twilight anesthesia and requires only two skin punctures for comprehensive sampling.

The company’s commercial model is direct enterprise field sales of the FDA-cleared Class II hardware to urology practices, hospitals, and ambulatory surgery centers, complemented by provider training and certification through a documented provider enrollment program and a patient-facing 'Find a PrecisionPoint Provider' locator that pulls demand toward trained sites. As of mid-2022, approximately 500 U.S. urologists had been trained to use the device, with the system in use across 13+ countries and roughly 70% transperineal biopsy penetration reported in the United Kingdom within two years. Perineologic operates with 1–10 employees, has not disclosed institutional funding, and is led by a commercial team drawn from Boston Scientific, Medtronic, Intuitive Surgical, and Smith+Nephew, with ten issued U.S. patents and five pending applications protecting both the current device and a pipeline of potential future products.

Perineologic firmographics

Firmographics
Name
Perineologic
Legal name
Perineologic
Website
https://perineologic.com
Company type
Private
Operating status
Operating
Headcount range
1–10 employees
Short description
Perineologic is a privately held medical device company that developed the FDA-cleared PrecisionPoint Transperineal Access System for freehand transperineal prostate biopsy, selling directly to urology practices and hospitals across 13+ countries.
Ownership category
akta.pro rank

Where Perineologic is headquartered

Location

Headquarters

HQ city
Cumberland
HQ country
United States
HQ region
North America

Offices1 record

Markets served

Perineologic business model

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

Revenue model

  1. PrecisionPoint Device Sales: Perineologic generates revenue through the sale of its PrecisionPoint Transperineal Access System medical devices to urology practices, hospitals, and healthcare systems. As a Class II medical device requiring FDA clearance, the product is sold directly to trained providers who perform prostate biopsies using the system.
  2. Provider Training and Certification: The company likely generates revenue through training and certification programs for urologists adopting the PrecisionPoint technique, though specific pricing for training services is not publicly disclosed.

Go-to-market motion2 records

Distribution channels3 records

Marketing channels6 records

Perineologic product offering

Product offering

Core offering

Perineologic develops, manufactures, and sells the PrecisionPoint Transperineal Access System (PPTAS), an FDA-cleared Class II medical device that enables urologists to perform freehand transperineal prostate biopsies through the perineum rather than the rectum. The system includes a patented clamping mechanism compatible with existing BK ultrasound platforms and cylindrical transducer probes, eliminating the need for bowel prep or antibiotics and reducing infection risk to nearly zero.

Product overview

Perineologic® is an innovative medical device company focused on developing and delivering technology to improve the safety, precision, and efficiency of healthcare options primarily in the field of urology. The company's core product is the PrecisionPoint® Transperineal Access System (PPTAS), which is the first FDA-cleared device enabling free-handed transperineal biopsy of the prostate. This system revolutionizes prostate biopsy methodology by allowing access through the perineum rather than the rectum, eliminating infection risks and enabling more comprehensive cancer detection. The PPTAS works in conjunction with existing ultrasound platforms (specifically BK ultrasound systems) and enables urologists to perform safer, more accurate prostate biopsies under local anesthesia.

Differentiator

Problem solved

Functional benefit

Brands

  • PrecisionPoint: The PrecisionPoint Transperineal Access System (PPTAS) - the first FDA cleared device allowing free-handed transperineal biopsy of the prostate. The device enables urologists to perform prostate biopsies through the perineum, avoiding the rectum entirely.

Products and services

  • PrecisionPoint® Transperineal Access System (PPTAS) FDA-cleared Class II medical device that enables free-handed transperineal biopsy of the prostate through the perineum, avoiding the rectum entirely. The system eliminates the need for bowel prep and antibiotics, reduces infection risk to nearly 0%, and allows comprehensive sampling of all prostate zones including the anterior region. The procedure takes 15-20 minutes and can be performed under local or twilight anesthesia. Designed for urologists performing prostate biopsies.

Quantifiable outcome

  • 94% of missed cancers after transrectal biopsies were located in the anterior region of the prostate, which PrecisionPoint can specifically target
  • +3 more outcomes

Companies that use Perineologic

Customer profile

Named customers3 records

Segments3 records

Ideal customer profiles3 records

Perineologic 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

Feature4 records

Perineologic partnerships and signals

Strategic signal

Partnerships

Two partnerships are on record, tiered core.

  • BK Medical (Analogic Corporation)coreTechnology or IntegrationPerineologic's PrecisionPoint system is designed to be compatible with BK ultrasound platforms and cylindrical transrectal ultrasound transducer probes (BK #8658 or equivalent). This integration allows urologists to use their existing BK ultrasound equipment with the PrecisionPoint device, reducing adoption barriers for practices already equipped with BK systems.
  • Urology Associates (Cumberland, MD)coreStrategic or Co-development PartnerDr. Matthew Allaway's urology practice served as the development and testing site for the PrecisionPoint technology. The practice, a 13,000-square-foot modern medical facility including clinical and research space and the Ambulatory Urologic Surgery Center, represents the foundational partnership where the technology was clinically developed over four years of development.

Scale indicators5 records

Recent moves6 records

Expansion highlights6 records

Perineologic competitors and assessment

Company assessment

Broad incumbents

  • Boston Scientific: Major medtech incumbent with a deep Urology/Pelvic Health portfolio including biopsy, ablation, and prostate diagnostics. Comparable because it is the dominant force in urology devices Perineologic sells into, and former Perineologic executives (Brasington, Tanksley, Tourtellot) all came from Boston Scientific roles.
  • Cook Medical: Long-established urology device manufacturer offering prostate biopsy needles, access devices, and procedure kits. Comparable because it competes for the same urology practice purchasing budgets and offers overlapping transrectal/transperineal biopsy supplies.
  • GE HealthCare (BK Medical): Owns BK Medical, whose ultrasound platforms and TRUS transducers are explicitly compatible with PrecisionPoint. Comparable as both a key integration partner and a potential broader competitor if it expands into procedure-specific access devices.
  • Philips (Invivo): Through Invivo, Philips provides MRI/ultrasound fusion-guided prostate biopsy solutions. Comparable as an alternative diagnostic biopsy workflow competing for urology department capital budgets and procedure referrals.
  • Intuitive Surgical: Dominant robotic surgery platform (da Vinci) used after prostate cancer diagnosis, often in conjunction with PrecisionPoint biopsies. Comparable because it shares the same urology ecosystem and a former Perineologic SVP previously held a Director, Key Accounts role at Intuitive.
  • Medtronic: Diversified medtech with urology and pelvic health offerings and a strong sales infrastructure into hospitals and ambulatory surgery centers. Comparable as a potential competitor with resources to enter transperineal access and a previous employer of Perineologic's SVP of Sales.
  • Hologic: Women's health and diagnostics leader that also serves urology through prostate biopsy and related diagnostics. Comparable because it competes for hospital/urology group purchasing decisions and has biopsy device capabilities.
  • Coloplast: Established urology and continence care company with prostate surgery and biopsy adjacencies. Comparable as a broader urology incumbent targeting the same clinical customers and could expand into transperineal access devices.

Direct peers

  • AngioDynamics: Medical device company with a dedicated prostate health business (NanoKnife, biopsy, and ablation technologies). Comparable because it sells directly to urology practices for prostate biopsy and focal therapy procedures, overlapping Perineologic's call point.

Emerging players

  • Biobot Surgical: Developer of robotic-assisted prostate biopsy and focal therapy devices (e.g., iSR'obot Mona Lisa). Comparable as a niche emerging competitor in the same transperineal biopsy category that PrecisionPoint addresses.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks6 records

Key highlights7 records

Customer concentration

Perineologic social profiles

Digital presence

Perineologic compliance and trust

Trust signal

Compliance1 record

Perineologic financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Perineologic leadership team

Management profile

Number of profiles

Profiles8 records

Perineologic funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

Perineologic M&A and investment

M&A and investment

M&A

Investments

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

Frequently asked questions about Perineologic

What does Perineologic do?

Perineologic develops, manufactures, and sells the PrecisionPoint Transperineal Access System (PPTAS), an FDA-cleared Class II medical device that enables urologists to perform freehand transperineal prostate biopsies through the perineum rather than the rectum. The system includes a patented clamping mechanism compatible with existing BK ultrasound platforms and cylindrical transducer probes, eliminating the need for bowel prep or antibiotics and reducing infection risk to nearly zero.

Is Perineologic a public or private company?

Perineologic is a private company. It is classified as founder individual operated bootstrapped and is currently operating.

When was Perineologic founded?

Perineologic was founded in -1. It employs 1 to 10 people.

Where is Perineologic based?

Perineologic is headquartered in Cumberland, United States, in the North America region.

How does Perineologic make money?

Two revenue lines are on record. PrecisionPoint Device Sales are the primary driver. The others are provider Training and Certification.

Who are Perineologic's main competitors?

Broad incumbents on record are Boston Scientific, Cook Medical, GE HealthCare (BK Medical), Philips (Invivo), Intuitive Surgical, Medtronic, Hologic and Coloplast. AngioDynamics is listed as a direct peer. Biobot Surgical is listed as an emerging player.

Does Perineologic have an API?

No public API is recorded for Perineologic.

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Live signals
PR NewswireLeading Prostate Biopsy Innovator Perineologic® Secures Significant Investment for Rapid ExpansionPerineologic, a pioneer in transperineal prostate biopsy technology headquartered in Cumberland, Maryland, has secured a strategic investment from a group of private equity and hedge fund executives. The capital infusion will be used to rapidly expand its commercial sales team and aggressively defend its patent portfolio protecting the PrecisionPoint® Transperineal Access System, which offers high cancer detection rates and low infection rates. The company also plans to expand its USA-based domestic manufacturing capabilities as part of its strategy to accelerate global market penetration.PR NewswirePerineologic Appoints Jim Fortune as President and Promotes Matthew Allaway, DO, to Chief Executive OfficerPerineologic, a subsidiary of Corbin Clinical Resources, Inc., announced the appointment of Jim Fortune as president and the promotion of Matthew Allaway, DO, to chief executive officer, with Fortune responsible for business strategy and operations and reporting to Dr. Allaway. Fortune brings more than 35 years of medical device industry experience, having previously served as COO at Ocular Therapeutix and in leadership roles at several companies acquired by Cardinal Health, Boston Scientific, Teleflex, Covidien, and Integra LifeSciences. Perineologic is focused on its PrecisionPoint Transperineal Access System for prostate cancer biopsy, which received FDA clearance in 2016 and is available in 14 countries.PR NewswirePerineologic Expands Leadership Team with Appointment of Evan Brasington as Chief Commercial OfficerPerineologic, a subsidiary of Corbin Clinical Resources, Inc., announced the appointment of Evan Brasington as Chief Commercial Officer to its executive leadership team. Brasington brings over 30 years of medical device sector experience, most recently serving as division vice president at Boston Scientific Corporation where he managed adoption of technologies acquired through deals including AMS, NxThera, and Augmenix. In this role, he will lead commercial strategy for the PrecisionPoint Transperineal Access System, the company's FDA-cleared and CE-marked medical device for freehand transperineal prostate cancer biopsies.