Orthalign, Inc
2 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 1 -5 REF:402566 component Lantern Knee recall (Z-1629-2026) | Orthalign, Inc | 2026-03-24 |
| Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 6-7 REF:402567 component Lantern Knee S recall (Z-1630-2026) | Orthalign, Inc | 2026-03-24 |
Track Orthalign, Inc automatically
Every clearance here is in the API, with alerts when new ones post.