Home › JENX LIMITED › Jenx
Jenx
JENX LIMITED · Model SB11-01 · UDI-DI 05056235209331
10
510(k) clearances
15
Adverse events (2 deaths)
1
Recalls
103
Facilities
Description
Support Pads Medium With Knee Strap Blue
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2003-05-30 | Chattanooga Corp. | Product contains an improper bracket for the transducer. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.