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FORCEPS

KLS-Martin L.P. · Model 09-023-02-07 · UDI-DI 00888118010643

EMG Prescription
10
510(k) clearances
11
Adverse events
1
Recalls
215
Facilities

Description

EXTRACTING, LOWER MOLAR, NO. 23, THIN PRONGS, 3 MM GAP

Recalls

DateFirmReason
2008-05-21Biomet Microfixation, Inc.The Biomet Microfixation Obwegeser Ramus Clamp, Wide Right 01-7996 were incorrectly etched as the left part number 01-7997.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.