Foundation Surgical Group
Country not established FDA establishment FEI 3039167712
- Devices
- 165
- Registrations
- FDA
- FDA recalls
- 0
What Foundation Surgical Group makes
The company designs and manufactures metallic spinal interbody fusion cages, including the Foundation Surgical Interwedge, for use in spinal fusion procedures.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.
Catalogue
Search and filter all 165 devicesShowing 1-50 of 165
Company details
- FDA FEI number
- 3039167712
- Address
- 7327 E Tierra Buena Ln Ste 101, Scottsdale, AZ, 85260
Frequently asked questions
How many devices does FOUNDATION SURGICAL GROUP have in the registry?
The registry currently lists 165 devices for FOUNDATION SURGICAL GROUP. Devices recorded under merged duplicate company entries are counted once.
Which registries list FOUNDATION SURGICAL GROUP's devices?
Among its 50 most recently registered devices, FOUNDATION SURGICAL GROUP has devices listed in FDA GUDID (50 devices).
What risk classes do FOUNDATION SURGICAL GROUP's devices fall under?
Among its 50 most recently registered devices, the classes recorded for FOUNDATION SURGICAL GROUP's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from FOUNDATION SURGICAL GROUP in the registry?
The most recently registered devices listed for FOUNDATION SURGICAL GROUP include Foundation Surgical Instruments FS50-010000, Foundation Surgical Interwedge FS50-020000, Foundation Surgical Interwedge FS50-100000 and Foundation Surgical Interwedge FS50-112200.