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Surgical Instrument

Jeil Medical Corporation · Model 20-QD-001 · UDI-DI 08809265158462

GXL Prescription
0
510(k) clearances
16
Adverse events
2
Recalls
17
Facilities

Recalls

DateFirmReason
2014-01-30Synthes, Inc.The CMF Battery Powered Driver graphic case contains outlines of the Battery Powered Driver, taps, screwdriver blades, and a screw holding sleeve. However, the device is not inten
2006-03-08Medtronic NeurosurgeryMedtronic Neurosurgery has initiated this action because it was determined that two lots of the Modular Screwdriver Blade components may exhiibt burrs along the tips of the Screwd

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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.