Home / Companies / Foundation Surgical Group, Inc.

Foundation Surgical Group, Inc.

FDA Regulatory Profile

Foundation Surgical Group, Inc. has 0 FDA recalls, 0 inspections, 5 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Jul 31, 2026

Reviewing Foundation Surgical Group, Inc. as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.

Check this supplier

Or check Foundation Surgical Group, Inc. yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.

Get a free API key

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances5Nov 8, 2026File dated Nov 2, 2026Current
Inspections0Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent 510(k) Clearances

K-NumberDeviceDate
K261810Vertiwedge® Intraosseous SystemJul 31, 2026
K261809Interwedge® Standalone LateralJul 31, 2026
K260011Foundation Surgical Navigated Lateral Disc Prep InstrumentsApr 16, 2026
K241468Vertiwedge® Intraosseous SystemNov 7, 2024
K241487Interwedge® Standalone LateralOct 2, 2024

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.