Avanti Orthopaedics, Inc.
Avanti Orthopaedics, Inc. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 9, 2026.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K261145 | Avanti Distal Elbow ORIF System | May 9, 2026 |
| K222967 | Avanti Orthopaedics 2.2mm and 2.7mm Cannulated Screws, Avanti Orthopaedics 3.2mm and 4.0mm Cannulate | Nov 23, 2022 |
| K211592 | Avanti Orthopaedics Ulnar Shortening System | Jul 16, 2021 |
| K191118 | Avanti Distal Radius and Forearm System | Dec 13, 2019 |