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Senolo
JIANGSU SENOLO MEDICAL TECHNOLOGY CO., LTD. · Model XB530 · UDI-DI 16952534421152
1
510(k) clearances
6
Adverse events
1
Recalls
64
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-02-27 | Emergency Products & Research | Failure of adhesive to secure the pole insert. |
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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.