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KENEX

KENEX (ELECTRO-MEDICAL) LIMITED · Model 314/05-01 · UDI-DI 05055449401883

IWX Prescription
3
510(k) clearances
1
Adverse events
1
Recalls
24
Facilities

Description

Mobile 1 Flap Flexible Shield 0.5mm Pb.

Recalls

DateFirmReason
2007-11-01Aadco Medical Inc.Screws may become loose from the mounted shield compromising stability

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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.