FDA Device Intelligence
HomeSynthes GmbH › NA

NA

Synthes GmbH · Model 495.414 · UDI-DI 10705034785707

EZXMQP Prescription
10
510(k) clearances
198
Adverse events (5 deaths)
1
Recalls
26
Facilities

Description

END RING 10MM DIA/2.5 DEG CONVEX (TI)

Recalls

DateFirmReason
2015-10-07Synthes (USA) Products LLCThe affected part number and lot listed above is incorrectly etched with the wrong part number and may not fit into a Small Fragment Plate.

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 docs
Data 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.