TYBR Health
Developer of a flowable, collagen-containing extracellular matrix hydrogel and a matched applicator system intended to reduce postoperative tendon adhesions and preserve tissue mobility. The organization reports preclinical efficacy and cadaver biomechanical safety testing and states it has progressed through the FDA 510(k) regulatory pathway.
Industries
Nr. of Employees
small (1-50)
Products
Flowable extracellular matrix hydrogel tendon protector and applicator system
A collagen-containing, decellularized ECM hydrogel formulated to be flowable at application, provide temporary biomechanical separation of healing tissues, modulate the local biology to support remodeling, and biodegrade over the normal healing timeline, paired with an applicator that mixes and precisely delivers the hydrogel intraoperatively.
B3 GEL System
A next-generation decellularized extracellular matrix (ECM) collagen-based gel system designed to prevent excessive scarring, provide biomechanical separation, and maintain natural tendon mobility during healing.
Flowable extracellular matrix hydrogel tendon protector and applicator system
A collagen-containing, decellularized ECM hydrogel formulated to be flowable at application, provide temporary biomechanical separation of healing tissues, modulate the local biology to support remodeling, and biodegrade over the normal healing timeline, paired with an applicator that mixes and precisely delivers the hydrogel intraoperatively.
B3 GEL System
A next-generation decellularized extracellular matrix (ECM) collagen-based gel system designed to prevent excessive scarring, provide biomechanical separation, and maintain natural tendon mobility during healing.
Expertise Areas
- Tendon repair and adhesion prevention
- Extracellular matrix biomaterials
- Surgical delivery systems for biomaterials
- Preclinical validation and biomechanical testing
Key Technologies
- Decellularized extracellular matrix hydrogel
- Thermally responsive flowable hydrogel
- On‑demand mixing and applicator delivery systems
- Colored formulations for intraoperative visualization
News & Updates
Reported preclinical results include improvements in range of motion and reductions in adhesion scores versus controls; data stated as on file and under review for publication.
Cadaver study evaluating mechanical safety of overapplication and effects on tendon gliding; concludes device can cover repairs while preserving mobility.
Company states it advanced from concept to FDA 510(k) clearance.
Reported preclinical results include improvements in range of motion and reductions in adhesion scores versus controls; data stated as on file and under review for publication.
Cadaver study evaluating mechanical safety of overapplication and effects on tendon gliding; concludes device can cover repairs while preserving mobility.
Company states it advanced from concept to FDA 510(k) clearance.