Home › Synthes GmbH › NA
NA
Synthes GmbH · Model 451.101 · UDI-DI 10887587054728
2
510(k) clearances
210
Adverse events
1
Recalls
52
Facilities
Description
2.0MM TI ADAPTION PLATE 20 HOLES/100MM-MALLEABLE
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2021-06-02 | Medtronic Neuromodulation | Excess nylon flash on the clip. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.