Contract manufacturerHYPERBRANCH MEDICAL TECHNOLOGY INC (Durham, NC)North CarolinaNeurologyClass III
HYPERBRANCH MEDICAL TECHNOLOGY INC
Contract manufacturer ยท Durham, NC
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3005920920 (openFDA record; or search FDA's registration database)
- FEI number
- 3005920920
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- STRYKER CORP. (FDA owner/operator no. 1811755)
- Registered address
- 800 CAPITOLA DR STE 12, Durham, NC 27713
- Contract listings
- 1 device listings, 1 product codes, first listed Oct 31, 2018
- Certification
- Not verified. We have no certification data for this facility yet.
Devices listed as contract work
Each row is an FDA product code this facility lists under its contract establishment type, with the date of its earliest such listing.
| Product code | Device (FDA name) | Class | Category | Role | First listed |
|---|
| NQR | Sealant, Dural | Class III | Neurology | Contract manufacturing | Oct 31, 2018 |
Other contract facilities of STRYKER CORP.
- Stryker Sustainability Solutions Phoenix, Phoenix, AZ
- POM Medical, LLC, Moorpark, CA
- TMJ Solutions, LLC, San Buenaventura, CA
- STRYKER CORP., Kalamazoo, MI
- STRYKER MANUFACTURING KALAMAZOO, Portage, MI
- HOWMEDICA OSTEONICS CORP, Mahwah, NJ
- STRYKER PUERTO RICO, LLC., Arroyo, PR
- WRIGHT MEDICAL TECHNOLOGY, INC., Arlington, TN
- Stryker Neurovascular, Salt Lake City, UT