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GSOURCE LLC · Model gS 26.0332 · UDI-DI 00840314209016

KAD
5
510(k) clearances
21
Adverse events
1
Recalls
120
Facilities

Description

Lempert Elevator 6 3/4", slightly ang, 2mm, sharp

Recalls

DateFirmReason
2024-12-03Sklar InstrumentsReports of various packaging issues that may result in a breach of the sterile barrier.

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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.