Footbridge Medical
Country not established
- Devices
- 1
What Footbridge Medical makes
Footbridge Medical makes the HyperFlex Bunion Correction System, a device designed for bunion correction procedures.
The HyperFlex Bunion Correction System is classified as a Class II medical device and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
HyperFlex™ Bunion Correction System Ref K241995
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Footbridge Medical have in the registry?
The registry currently lists 1 device for Footbridge Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Footbridge Medical's devices?
Among its 1 most recently registered device, Footbridge Medical has devices listed in FDA 510(k) (1 device).
What risk classes do Footbridge Medical's devices fall under?
Among its 1 most recently registered device, the classes recorded for Footbridge Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Footbridge Medical in the registry?
The most recently registered devices listed for Footbridge Medical include HyperFlex™ Bunion Correction System.