Aevumed, Inc.
Aevumed, Inc. appears in FDA public data with 0 recalls, 8 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on September 2, 2026.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K253065 | Aevumed SUPERCYNCH Button System | September 2, 2026 |
| K254306 | Aevumed FENIX Suture Anchor | March 4, 2026 |
| K260004 | Aevumed PROTEKT Suture Anchor | January 28, 2026 |
| K253040 | Aevumed FASE Suture Anchor | October 21, 2025 |
| K242895 | Aevumed PHANTOM Suture Anchors | August 6, 2025 |
| K223878 | Aevumed RAPID Suture Anchors | March 17, 2023 |
| K222363 | Aevumed PHANTOM-LP Suture Anchors | November 28, 2022 |
| K180464 | AEVUMED PHANTOM Suture Anchors | May 31, 2018 |