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ENT Sinus
Smith & Nephew, Inc. · Model 602-00210 · UDI-DI 00817470009767
LYA
Prescription
1
510(k) clearances
203
Adverse events (3 deaths)
2
Recalls
106
Facilities
Description
MEDIENT MIDDLE TURBINATE IMPLANT 4-PACK
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-07-27 | GELITA MEDICAL GMBH | In routine bioburden testing, higher than acceptable levels of Endotoxins were observed. |
| 2006-07-11 | Porex Surgical, Inc. | Device contains a trace amount of amine via introduction through an intermediate supplied by a third party raw material |
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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.