Foundation Surgical Group, Inc.
Foundation Surgical Group, Inc. appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 31, 2026.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K261810 | Vertiwedge® Intraosseous System | July 31, 2026 |
| K261809 | Interwedge® Standalone Lateral | July 31, 2026 |
| K260011 | Foundation Surgical Navigated Lateral Disc Prep Instruments | April 16, 2026 |
| K241468 | Vertiwedge® Intraosseous System | November 7, 2024 |
| K241487 | Interwedge® Standalone Lateral | October 2, 2024 |