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LEVEL ONE CMF
KLS-Martin L.P. · Model 50-173-03-91 · UDI-DI 00888118073501
NEI
Prescription
7
510(k) clearances
24
Adverse events
0
Recalls
15
Facilities
Description
SCREW, CROSSDRIVE, TLCK, FASTENING, TEMPORARY CONDYLAR IMPLANT, TI-6AL-4V
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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData 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.