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DiagnosTear

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Namestring
DiagnosTear
Legal namestring
DiagnosTear Technologies Inc.
Company typeenum
Public
Founded yearint
2013
Descriptiontext

DiagnosTear Technologies Inc. (CSE:DTR; Frankfurt-listed) is an Israel-based, clinical-to-commercial-stage ophthalmic diagnostics company developing the TeaRx™ platform, a point-of-care system that performs multi-parameter analysis of tear fluid for eye disease diagnosis and monitoring. The platform is built around a proprietary single-use microfluidic tear collector that captures approximately one microliter of tear fluid with a color-change sampling indicator, followed by a semi-quantitative multi-parameter immunoassay and a cloud-based interpretive readout; the full procedure is reported to take under ten minutes. The first cleared product, TeaRx Dry Eye, holds CE-IVD and Israeli Ministry of Health (AMAR) approvals and is offered in 3-parameter and 5-parameter versions, with company-reported clinical performance of 86% sensitivity and 87% specificity for high-severity disease and ≥94% prediction of Cyclosporine A treatment responsiveness validated in a 600-subject study. A pipeline product, TeaRx Red Eye, is positioned as a first-of-its-kind differential test for adenoviral conjunctivitis, Herpetic Keratitis and allergic conjunctivitis, with manufacturing tooling for 100,000 units completed in early 2025 and clinical studies underway in France (AlyaTec), India (LV Prasad Eye Institute) and Israel.

The company sells diagnostic devices and consumable tear collectors to healthcare providers — primarily ophthalmologists for dry eye management and primary care physicians (GPs, family practitioners, pediatricians) for red eye differential diagnosis — with additional targeting of pharmaceutical companies and CROs (e.g., Lexitas Pharma Services) for use in ophthalmic clinical trials as a patient stratification and treatment-response biomarker. The revenue model is device-plus-consumable (single-use tear collectors) sold B2B, which the company describes as one-time per test/device sale with recurring consumable pull-through potential. Go-to-market is a hybrid of direct enterprise sales and regional channel partnerships, illustrated by the February 2026 Letter of Intent with UK-based Hanson Medical for UK distribution and engagement of bullVestor Medien GmbH for European marketing. The company became public in February 2024 via a Reverse Takeover transaction and commenced CSE trading in December 2024, subsequently listing on the Frankfurt Stock Exchange in October 2025.

Short descriptiontext

DiagnosTear Technologies Inc. develops and commercializes the TeaRx point-of-care tear-fluid diagnostic platform for ophthalmic disease, serving ophthalmologists, primary care physicians and ophthalmic clinical trials with CE-IVD-cleared dry eye and red eye tests.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1–10
akta.pro rankint
HeadquartersTel Aviv, Israel
HQ citystring
Tel Aviv
HQ countrystring
Israel
HQ regionstring
Middle East
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
ophthalmic diagnostics, tear fluid analysis, point-of-care testing, dry eye diagnosis, microfluidic immunoassay
Industry1 code
1Dry Eye & Ocular Surface Devices (Meibography, Tear Osmolarity, IPL, Thermal Pulsation)
CodeHLAHAJAFPrimaryYes
NAICS code1 code
  • Electromedical and Electrotherapeutic Apparatus Manufacturing334510
SIC code2 codes
  • Surgical & Medical Instruments & Apparatus3841
  • In Vitro & In Vivo Diagnostic Substances2835
Product category
Ophthalmic Diagnostics
Social media profiles2 records
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model1 record
1Diagnostic Device Sales
TypeOne Time License
Description

DiagnosTear generates revenue through the sale of its TeaRx diagnostic devices and proprietary tear collectors. The company sells point-of-care diagnostic tests for dry eye syndrome and red eye conditions. Revenue is one-time per test/device sale, with potential for recurring purchases as the tear collector is single-use.

diagnostear.com
Marketing channels8 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

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

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

Diagnostic platform for point-of-care testing of ophthalmic pathologies through multi-parameter composition analysis of tear fluid, including TeaRx Dry Eye and TeaRx Red Eye products.

diagnostear.com
Core offering1 text field

DiagnosTear develops and commercializes the TeaRx™ point-of-care diagnostic platform that analyzes tear fluid to identify, monitor, and stratify ophthalmic conditions such as Dry Eye Syndrome and red eye pathologies. The platform combines a proprietary single-use microfluidic tear collector with a multi-parameter immunoassay and cloud-based algorithm interpretation, delivering results in under 10 minutes for use by ophthalmologists and primary care physicians.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 5 values shown
  • 86% sensitivity and 87% specificity for detection of high severity Dry Eye Syndrome
+4 more records
Product overview1 text field

DiagnosTear offers the TeaRx™ platform as its core diagnostic technology. The platform consists of TeaRx™ Dry Eye (CE-IVD approved test for identification and monitoring of Dry Eye Syndrome), TeaRx™ Red Eye (differential diagnosis of adenoviral conjunctivitis, Herpetic Keratitis, and Allergic conjunctivitis), and the TeaRx™ Tear Collector (proprietary microfluidic tear collection device). The TeaRx platform uses tear fluid analysis with multi-parameter immunoassays and cloud-based algorithmic interpretation, with the whole procedure taking less than 10 minutes.

Product and service3 records
1TeaRx Dry Eye
CategoryOphthalmic diagnostic test
Description

The first CE-IVD approved point-of-care test based on the TeaRx platform, intended for the identification and monitoring of Dry Eye Syndrome (DES). Available in 3-parameter and 5-parameter versions, with clinical trials demonstrating 86% sensitivity and 87% specificity for detection of high severity DES, ≥80% sensitivity for differentiating severe vs. non-severe Dry Eye, and ≥94% prediction of Cyclosporine A responsiveness at baseline. Targeted at ophthalmologists and eye-care specialists.

2TeaRx Red Eye
CategoryOphthalmic diagnostic test
Description

The first test of its kind for differential assessment of adenoviral conjunctivitis, Herpetic Keratitis, and allergic conjunctivitis using tear fluid analysis. Designed for use by primary care physicians, family practitioners, pediatricians, and ophthalmologists to enable on-site differentiation of viral vs. allergic red eye without requiring referral. Clinical trials are underway in India (LV Prasad Eye Institute), France (AlyaTec), and with Sun Pharma and Israel's largest HMO.

3TeaRx Tear Collector
CategoryMicrofluidic sample-collection consumable
Description

DiagnosTear's proprietary single-use microfluidic tear collector that is an integral part of the TeaRx technology. Allows simple, non-invasive collection of 1 microliter of tear fluid and subsequent dilution in assay buffer, with proper sampling ensured by a color change (from brown to yellow) on the tip of the micro-capillary. Offered as a standalone consumable component.

Scale indicator8 records

Each record includes

Type, Value, Description, Source

Partnership6 partners
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-02-26
Description

Clinical study collaboration with French CRO AlyaTec following regulatory and ethics approvals from French authorities (ANSM and the French Ethics Committee). The study evaluates total tear IgE as a biomarker for Allergic Conjunctivitis using the TeaRx™ Red Eye diagnostic platform. Patient recruitment and sampling have commenced to finalize analytical validation supporting the FDA submission pathway.

Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2026-02-20
Description

Non-binding Letter of Intent to explore commercial partnership for the TeaRx™ dry-eye diagnostic platform in the United Kingdom under a defined period until May 15, 2026. During the LOI period, Hanson Medical conducts market evaluation activities and engages with eye-care professionals to assess clinical integration and commercial adoption pathways. The initiative is part of DiagnosTear's strategy to build localized partnerships in key European markets and may lead to a definitive commercial agreement.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2023-09-13
Description

Partnership for the use of TeaRx™ in ophthalmic clinical trials. Lexitas Pharma Services provides clinical research services and incorporates TeaRx tear-based diagnostics for patient stratification and treatment response measurement in clinical studies.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Clinical trials partnership for TeaRx Red Eye development conducted in partnership with LV Prasad Eye Institute in India. LV Prasad Eye Institute is a leading eye care institution providing research collaboration for clinical validation of tear-based diagnostic tests.

Strategic tierMinorTypeStrategic or Co-development Partner
Description

Partnership mentioned for TeaRx Red Eye development alongside other clinical collaborations. Sun Pharma is a pharmaceutical company involved in ophthalmic treatments.

6Israel's Largest Health Maintenance Organization
Strategic tierMinorTypeStrategic or Co-development Partner
Description

Clinical trial partnership for TeaRx Red Eye with Israel's largest Health Maintenance Organization for tear-based diagnostic development.

stockhouse.com
Recent move9 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Market position
Competitive moat3 records

Each record includes

Type, Details

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

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

AI maturity
App detail

Has app

Feature5 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles13 records

Each record includes

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

No data
Compliance3 records

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds1 record

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 →

DiagnosTear

Ophthalmic Diagnosticsdiagnostear.com

DiagnosTear Technologies Inc. develops and commercializes the TeaRx point-of-care tear-fluid diagnostic platform for ophthalmic disease, serving ophthalmologists, primary care physicians and ophthalmic clinical trials with CE-IVD-cleared dry eye and red eye tests.

What DiagnosTear does

DiagnosTear Technologies Inc. (CSE:DTR; Frankfurt-listed) is an Israel-based, clinical-to-commercial-stage ophthalmic diagnostics company developing the TeaRx™ platform, a point-of-care system that performs multi-parameter analysis of tear fluid for eye disease diagnosis and monitoring. The platform is built around a proprietary single-use microfluidic tear collector that captures approximately one microliter of tear fluid with a color-change sampling indicator, followed by a semi-quantitative multi-parameter immunoassay and a cloud-based interpretive readout; the full procedure is reported to take under ten minutes. The first cleared product, TeaRx Dry Eye, holds CE-IVD and Israeli Ministry of Health (AMAR) approvals and is offered in 3-parameter and 5-parameter versions, with company-reported clinical performance of 86% sensitivity and 87% specificity for high-severity disease and ≥94% prediction of Cyclosporine A treatment responsiveness validated in a 600-subject study. A pipeline product, TeaRx Red Eye, is positioned as a first-of-its-kind differential test for adenoviral conjunctivitis, Herpetic Keratitis and allergic conjunctivitis, with manufacturing tooling for 100,000 units completed in early 2025 and clinical studies underway in France (AlyaTec), India (LV Prasad Eye Institute) and Israel.

The company sells diagnostic devices and consumable tear collectors to healthcare providers — primarily ophthalmologists for dry eye management and primary care physicians (GPs, family practitioners, pediatricians) for red eye differential diagnosis — with additional targeting of pharmaceutical companies and CROs (e.g., Lexitas Pharma Services) for use in ophthalmic clinical trials as a patient stratification and treatment-response biomarker. The revenue model is device-plus-consumable (single-use tear collectors) sold B2B, which the company describes as one-time per test/device sale with recurring consumable pull-through potential. Go-to-market is a hybrid of direct enterprise sales and regional channel partnerships, illustrated by the February 2026 Letter of Intent with UK-based Hanson Medical for UK distribution and engagement of bullVestor Medien GmbH for European marketing. The company became public in February 2024 via a Reverse Takeover transaction and commenced CSE trading in December 2024, subsequently listing on the Frankfurt Stock Exchange in October 2025.

DiagnosTear firmographics

Firmographics
Name
DiagnosTear
Legal name
DiagnosTear Technologies Inc.
Website
http://www.diagnostear.com
Company type
Public
Founded year
2013
Operating status
Operating
Headcount range
1–10 employees
Short description
DiagnosTear Technologies Inc. develops and commercializes the TeaRx point-of-care tear-fluid diagnostic platform for ophthalmic disease, serving ophthalmologists, primary care physicians and ophthalmic clinical trials with CE-IVD-cleared dry eye and red eye tests.
Ownership category
akta.pro rank

DiagnosTear industry classification

Industry
Product category
Ophthalmic Diagnostics
NAICS
Electromedical and Electrotherapeutic Apparatus Manufacturing (334510)
SIC
Surgical & Medical Instruments & Apparatus (3841), In Vitro & In Vivo Diagnostic Substances (2835)
akta.pro primary industry
Dry Eye & Ocular Surface Devices (Meibography, Tear Osmolarity, IPL, Thermal Pulsation) (HLAHAJAF)

Keywords

  • Ophthalmic diagnostics
  • Tear fluid analysis
  • Point-of-care testing
  • Dry eye diagnosis
  • Microfluidic immunoassay

Where DiagnosTear is headquartered

Location

Headquarters

HQ city
Tel Aviv
HQ country
Israel
HQ region
Middle East

Offices1 record

Markets served

DiagnosTear business model

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

Revenue model

  1. Diagnostic Device Sales: DiagnosTear generates revenue through the sale of its TeaRx diagnostic devices and proprietary tear collectors. The company sells point-of-care diagnostic tests for dry eye syndrome and red eye conditions. Revenue is one-time per test/device sale, with potential for recurring purchases as the tear collector is single-use.

Go-to-market motion2 records

Distribution channels1 record

Marketing channels8 records

DiagnosTear product offering

Product offering

Core offering

DiagnosTear develops and commercializes the TeaRx™ point-of-care diagnostic platform that analyzes tear fluid to identify, monitor, and stratify ophthalmic conditions such as Dry Eye Syndrome and red eye pathologies. The platform combines a proprietary single-use microfluidic tear collector with a multi-parameter immunoassay and cloud-based algorithm interpretation, delivering results in under 10 minutes for use by ophthalmologists and primary care physicians.

Product overview

DiagnosTear offers the TeaRx™ platform as its core diagnostic technology. The platform consists of TeaRx™ Dry Eye (CE-IVD approved test for identification and monitoring of Dry Eye Syndrome), TeaRx™ Red Eye (differential diagnosis of adenoviral conjunctivitis, Herpetic Keratitis, and Allergic conjunctivitis), and the TeaRx™ Tear Collector (proprietary microfluidic tear collection device). The TeaRx platform uses tear fluid analysis with multi-parameter immunoassays and cloud-based algorithmic interpretation, with the whole procedure taking less than 10 minutes.

Differentiator

Problem solved

Functional benefit

Brands

  • TeaRx: Diagnostic platform for point-of-care testing of ophthalmic pathologies through multi-parameter composition analysis of tear fluid, including TeaRx Dry Eye and TeaRx Red Eye products.

Products and services

  • TeaRx Dry Eye The first CE-IVD approved point-of-care test based on the TeaRx platform, intended for the identification and monitoring of Dry Eye Syndrome (DES). Available in 3-parameter and 5-parameter versions, with clinical trials demonstrating 86% sensitivity and 87% specificity for detection of high severity DES, ≥80% sensitivity for differentiating severe vs. non-severe Dry Eye, and ≥94% prediction of Cyclosporine A responsiveness at baseline. Targeted at ophthalmologists and eye-care specialists.
  • TeaRx Red Eye The first test of its kind for differential assessment of adenoviral conjunctivitis, Herpetic Keratitis, and allergic conjunctivitis using tear fluid analysis. Designed for use by primary care physicians, family practitioners, pediatricians, and ophthalmologists to enable on-site differentiation of viral vs. allergic red eye without requiring referral. Clinical trials are underway in India (LV Prasad Eye Institute), France (AlyaTec), and with Sun Pharma and Israel's largest HMO.
  • TeaRx Tear Collector DiagnosTear's proprietary single-use microfluidic tear collector that is an integral part of the TeaRx technology. Allows simple, non-invasive collection of 1 microliter of tear fluid and subsequent dilution in assay buffer, with proper sampling ensured by a color change (from brown to yellow) on the tip of the micro-capillary. Offered as a standalone consumable component.

Quantifiable outcome

  • 86% sensitivity and 87% specificity for detection of high severity Dry Eye Syndrome
  • +4 more outcomes

Companies that use DiagnosTear

Customer profile

Segments3 records

Ideal customer profiles3 records

DiagnosTear technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature5 records

DiagnosTear partnerships and signals

Strategic signal

Partnerships

Six partnerships are on record, tiered core and minor.

  • AlyaTeccoreStrategic or Co-development Partner · 26 February 2026Clinical study collaboration with French CRO AlyaTec following regulatory and ethics approvals from French authorities (ANSM and the French Ethics Committee). The study evaluates total tear IgE as a biomarker for Allergic Conjunctivitis using the TeaRx™ Red Eye diagnostic platform. Patient recruitment and sampling have commenced to finalize analytical validation supporting the FDA submission pathway.
  • Hanson MedicalcoreChannel Partner/ Reseller/ Distributor · 20 February 2026Non-binding Letter of Intent to explore commercial partnership for the TeaRx™ dry-eye diagnostic platform in the United Kingdom under a defined period until May 15, 2026. During the LOI period, Hanson Medical conducts market evaluation activities and engages with eye-care professionals to assess clinical integration and commercial adoption pathways. The initiative is part of DiagnosTear's strategy to build localized partnerships in key European markets and may lead to a definitive commercial agreement.
  • Lexitas Pharma Services, Inc.coreStrategic or Co-development Partner · 13 September 2023Partnership for the use of TeaRx™ in ophthalmic clinical trials. Lexitas Pharma Services provides clinical research services and incorporates TeaRx tear-based diagnostics for patient stratification and treatment response measurement in clinical studies.
  • LV Prasad Eye InstitutecoreStrategic or Co-development PartnerClinical trials partnership for TeaRx Red Eye development conducted in partnership with LV Prasad Eye Institute in India. LV Prasad Eye Institute is a leading eye care institution providing research collaboration for clinical validation of tear-based diagnostic tests.
  • Sun PharmaminorStrategic or Co-development PartnerPartnership mentioned for TeaRx Red Eye development alongside other clinical collaborations. Sun Pharma is a pharmaceutical company involved in ophthalmic treatments.
  • Israel's Largest Health Maintenance OrganizationminorStrategic or Co-development PartnerClinical trial partnership for TeaRx Red Eye with Israel's largest Health Maintenance Organization for tear-based diagnostic development.

Scale indicators8 records

Recent moves9 records

Expansion highlights6 records

DiagnosTear competitors and assessment

Company assessment

Market position

Competitive moat3 records

Key highlights7 records

Customer concentration

DiagnosTear social profiles

Digital presence

DiagnosTear compliance and trust

Trust signal

Compliance3 records

DiagnosTear financial estimates

Financial estimate

Revenue estimate

Valuation estimate

DiagnosTear leadership team

Management profile

Number of profiles

Profiles13 records

DiagnosTear funding detail

Funding detail

Funding overview

Funding rounds1 record

Investors

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

DiagnosTear 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 DiagnosTear

What does DiagnosTear do?

DiagnosTear develops and commercializes the TeaRx™ point-of-care diagnostic platform that analyzes tear fluid to identify, monitor, and stratify ophthalmic conditions such as Dry Eye Syndrome and red eye pathologies. The platform combines a proprietary single-use microfluidic tear collector with a multi-parameter immunoassay and cloud-based algorithm interpretation, delivering results in under 10 minutes for use by ophthalmologists and primary care physicians.

Is DiagnosTear a public or private company?

DiagnosTear is a public company. It is classified as public and is currently operating.

When was DiagnosTear founded?

DiagnosTear was founded in 2013. It employs 1 to 10 people.

Where is DiagnosTear based?

DiagnosTear is headquartered in Tel Aviv, Israel, in the Middle East region.

How does DiagnosTear make money?

One revenue line is on record: diagnostic Device Sales.

Does DiagnosTear have an API?

No public API is recorded for DiagnosTear.

What industry is DiagnosTear in?

DiagnosTear's product category is Ophthalmic Diagnostics. Its primary akta.pro industry code is HLAHAJAF, Dry Eye & Ocular Surface Devices (Meibography, Tear Osmolarity, IPL, Thermal Pulsation). Its NAICS code is 334510 and its SIC code is 3841.

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Live signals
MarketScreenerDiagnosTear Technologies Submits Pre-Submission Request to FDA for TeaRx Red Eye Diagnostic TestDiagnosTear Technologies, an Israel-based ophthalmic diagnostics firm, submitted a pre-submission request to the FDA for its TeaRx red eye diagnostic test. The company develops tear-fluid analytical platforms for monitoring front-of-the-eye diseases, with R&D supported by government-funded programs.NewsfileDiagnosTear Technologies Announces FDA Pre-Submission for TeaRx(TM) Red Eye Diagnostic TestDiagnosTear Technologies submitted a pre-submission request to the FDA for its TeaRx Red Eye diagnostic test. The test is a rapid point-of-care test to differentiate adenoviral conjunctivitis, HSV infection, and allergic conjunctivitis in red-eye patients. The company seeks FDA input on the regulatory pathway and data development plan.NewsfileDiagnosTear Technologies Inc. Announces Private Placement of UnitsDiagnosTear Technologies Inc. announced a non-brokered private placement of up to 2.8 million units at C$0.50 each, raising up to C$1.4 million in gross proceeds. The units include a common share and a warrant exercisable at C$1.00, with net proceeds for working capital and general corporate purposes.NewsfileDiagnosTear Achieves Major Scientific Milestone with Publication of TeaRx(TM) Clinical Study in Current Eye Research JournalDiagnosTear Technologies published its TeaRx clinical study in Current Eye Research, evaluating the platform in about 500 Dry Eye Disease patients and 100 controls. The study found TeaRx could stratify disease severity and predict responsiveness to Cyclosporine A therapy. The company is offering test kits to collaborators and considering LDT validation.NewsfileRETRANSMISSION: DiagnosTear Secures Exclusive Global Rights to CLARIFY Eye Imaging Platform for Needle-Free Blood DiagnosticsDiagnosTear entered a definitive exclusive global license agreement on May 12, 2026, to commercialize CLARIFY, an eye-based platform for needle-free blood diagnostics. The agreement includes a 3% royalty on net sales up to $20M and 4% thereafter, with sublicensing revenue shares. The company will lead development and clinical validation.NewsfileDiagnosTear Secures Exclusive Global Rights to CLARIFY Eye Imaging Platform for Needle-Free Blood DiagnosticsDiagnosTear entered an exclusive global license agreement with Sheba Impact and Ramot to commercialize CLARIFY, an eye-based platform for needle-free blood diagnostics. The deal includes 3% royalties on net sales up to $20M and 4% thereafter, with sublicensing revenue shares. DiagnosTear will lead development and clinical validation.NewsfileDiagnosTear Technologies Inc. Announces Results of AGMDiagnosTear Technologies Inc. held its annual general meeting on May 7, 2026, and shareholders approved all management recommendations. The company elected five directors, appointed Doane Grant Thornton LLP as auditor, and confirmed its rolling 10% equity incentive plan. The company's TeaRx platform is developing tests for ophthalmic conditions, with the first CE-IVD for dry eye syndrome not yet FDA-cleared.NewsfileDiagnosTear Technologies Inc. Announces Warrant ExtensionDiagnosTear Technologies extended the expiry of its November 2024 and December 2024 common share purchase warrants by six months, to November 20, 2026 and December 2, 2026, respectively. The exercise price remains $1.00, and no action is required from warrant holders.NewsfileDiagnosTear Technologies Inc. Announces Adoption of Semi-Annual ReportingDiagnosTear Technologies Inc. adopted a semi-annual financial reporting framework effective immediately under British Columbia's CBO 51-933. The company will not file interim reports for Q1 and Q3 2026, continuing annual and six-month reports. It confirms eligibility as a venture issuer with revenues under $10 million.NewsfileDiagnosTear Announces Regulatory Approvals in France and Study Initiation with AlyaTec for TeaRx(TM) Red EyeDiagnosTear Technologies Inc. has received regulatory and ethics approvals from French authorities (ANSM and the French Ethics Committee) to proceed with a clinical study for its TeaRx™ Red Eye diagnostic platform. The company, in collaboration with French CRO AlyaTec, has commenced patient recruitment and sampling to evaluate total tear IgE as a biomarker for Allergic Conjunctivitis. This study aims to finalize analytical validation supporting the FDA submission pathway for the diagnostic test.