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Surgical Instrument

Jeil Medical Corporation · Model 111-083-L · UDI-DI 08809282819957

PBF Prescription
1
510(k) clearances
225
Adverse events
0
Recalls
35
Facilities

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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.