Skip to content

Foundation Surgical Group

Also registered as Foundation Surgical Group, Inc.

United Statesfrom the FDA registration address 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.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue165

Newest first, rows 151-165 of 165

Search and filter all 165 devices
Skip device list

Rows 151-165 of 165

Showing 151-165 of 165

Company details

FDA FEI number
3039167712
Address
7327 E Tierra Buena Ln Ste 101, Scottsdale, AZ, 85260

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.