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Sklar

SKLAR CORPORATION · Model 49-4727 · UDI-DI 10649111444005

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

Description

KLEIN EX FCP W SPRING CV, PTD

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.