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KENEX
KENEX (ELECTRO-MEDICAL) LIMITED · Model 310/B-3 · UDI-DI 05055449401807
IWX
Prescription
3
510(k) clearances
1
Adverse events
1
Recalls
24
Facilities
Description
Mobile 'SEE-THRU' Adjustable Shield
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2007-11-01 | Aadco Medical Inc. | Screws may become loose from the mounted shield compromising stability |
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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.