FDA Device Intelligence
HomeSynthes GmbH › LCP

LCP

Synthes GmbH · Model SD238.008 · UDI-DI 10886982003164

KTW Prescription
1
510(k) clearances
910
Adverse events
57
Recalls
51
Facilities

Description

4.5MM LCP ANGLE BLADE PLATE 130 DEGREES 1 HOLE 85MM BLADE

Recalls

DateFirmReason
2010-10-27Synthes USA (HQ), Inc.Potential for out of specification star grind teeth.
2010-10-27Synthes USA (HQ), Inc.Potential for out of specification star grind teeth.
2010-10-27Synthes USA (HQ), Inc.Potential for out of specification star grind teeth.
2010-10-27Synthes USA (HQ), Inc.Potential for out of specification star grind teeth.
2010-10-27Synthes USA (HQ), Inc.Potential for out of specification star grind teeth.
2010-10-27Synthes USA (HQ), Inc.Potential for out of specification star grind teeth.
2010-10-27Synthes USA (HQ), Inc.Potential for out of specification star grind teeth.
2010-10-27Synthes USA (HQ), Inc.Potential for out of specification star grind teeth.
2010-10-27Synthes USA (HQ), Inc.Potential for out of specification star grind teeth.
2010-10-27Synthes USA (HQ), Inc.Potential for out of specification star grind teeth.

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.