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Jenx
JENX LIMITED · Model SL3P-03 · UDI-DI 05056235201151
10
510(k) clearances
15
Adverse events (2 deaths)
1
Recalls
103
Facilities
Description
Side Lying Board Size 3 Green
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2003-05-30 | Chattanooga Corp. | Product contains an improper bracket for the transducer. |
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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.