Trinity Orthopedics, LLC
United Statesfrom the FDA registration address FDA establishment FEI 3006700424
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
What Trinity Orthopedics, LLC makes
Trinity Orthopedics, LLC makes pedicle screw systems, specifically the Single Planar Multi Axial (SPMA) Pedicle Screw System and modifications to that system.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3006700424
- Address
- 8817 Production Ave., San Diego, CA, 92121
Frequently asked questions
How many devices does TRINITY ORTHOPEDICS, LLC have in the registry?
The registry currently lists 2 devices for TRINITY ORTHOPEDICS, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list TRINITY ORTHOPEDICS, LLC's devices?
Among its 2 most recently registered devices, TRINITY ORTHOPEDICS, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do TRINITY ORTHOPEDICS, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for TRINITY ORTHOPEDICS, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from TRINITY ORTHOPEDICS, LLC in the registry?
The most recently registered devices listed for TRINITY ORTHOPEDICS, LLC include SINGLE PLANAR MULTI AXIAL (SPMA) PEDICLE SCREW SYSTEM and MODIFICATION TO SINGLE PLANAR MULTI AXIS (SPMA) PEDICLE SCREW SYSTEM.