Orthonovis, Inc.
Orthonovis, 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 Oct 2, 2025.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K252758 | Cannulated Screw and Kirschner (K wire) System | Oct 2, 2025 |
| K250498 | BPS Wrist Fracture System | Mar 17, 2025 |
| K250055 | BPS - Bone Fragment Fixation Plates, Screws and Washers | Feb 6, 2025 |
| K242343 | BPS Wrist Fracture System | Oct 4, 2024 |
| K213905 | ONX Large External Fixation System | Aug 25, 2022 |