Matrix Surgical USA
Country not established
- Devices
- 1
What Matrix Surgical USA makes
Matrix Surgical USA manufactures OMNIPORE surgical implants and related accessories, designed for use in orthopedic and spinal procedures. These products include components intended for internal fixation, such as plates, screws, and cages, to support bone stabilization and spinal fusion.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) pathway. The devices are listed in the FDA’s 510(k) database, and the company is headquartered in the United States.
Catalogue
Omnipore Surgical Implants And Accessories Ref K123908
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Matrix Surgical USA have in the registry?
The registry currently lists 1 device for Matrix Surgical USA. Devices recorded under merged duplicate company entries are counted once.
Which registries list Matrix Surgical USA's devices?
Among its 1 most recently registered device, Matrix Surgical USA has devices listed in FDA 510(k) (1 device).
What risk classes do Matrix Surgical USA's devices fall under?
Among its 1 most recently registered device, the classes recorded for Matrix Surgical USA's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Matrix Surgical USA in the registry?
The most recently registered devices listed for Matrix Surgical USA include OMNIPORE SURGICAL IMPLANTS AND ACCESSORIES.