Rigid FX Orthopedics, Incorporated
United StatesFDA applicant, unverified
- Devices
- 2
What Rigid FX Orthopedics, Incorporated makes
Rigid FX Orthopedics, Incorporated manufactures external fixation devices, including the CLEARVIEW WRIST FIXATOR and EXTERNAL FIXATION RING, designed for orthopedic stabilization of bone fractures or deformities.
These products are classified as Class II devices under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Clearview Wrist Fixator Ref K020311
Regimes: 510(k) Registry: 510(k)External Fixation Ring Ref K022423
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rigid FX Orthopedics, Incorporated have in the registry?
The registry currently lists 2 devices for Rigid FX Orthopedics, Incorporated. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rigid FX Orthopedics, Incorporated's devices?
Among its 2 most recently registered devices, Rigid FX Orthopedics, Incorporated has devices listed in FDA 510(k) (2 devices).
What risk classes do Rigid FX Orthopedics, Incorporated's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Rigid FX Orthopedics, Incorporated's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rigid FX Orthopedics, Incorporated in the registry?
The most recently registered devices listed for Rigid FX Orthopedics, Incorporated include CLEARVIEW WRIST FIXATOR and EXTERNAL FIXATION RING.