FDA Device Intelligence
Home › KLS-Martin L.P. › FORCEPS

FORCEPS

KLS-Martin L.P. · Model 12-610-02-07 · UDI-DI 00888118017697

GZX Prescription
10
510(k) clearances
67
Adverse events (1 deaths)
1
Recalls
137
Facilities

Description

JANETTA, BAYONET, ANGLED UP

Recalls

DateFirmReason
2007-01-22Medtronic Xomed, Inc.A labeling discrepancy was internally identified for the surface electrode component of REF 8263210 AccuGuide EMG Injection Needle, 30G X 25MM. The outside box label correctly ind

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.