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Implantable Transprostatic Tissue Retractor System
FDA product code PEW · Class 2 · Gastroenterology, Urology
27
Registered devices
471
Adverse events
2
Recalls
11
510(k) clearances
Devices with this code
UroLift — NEOTRACT, INC.UROLIFT — TELEFLEX INCORPORATEDUROLIFT — TELEFLEX INCORPORATEDUROLIFT — TELEFLEX INCORPORATEDUROLIFT — TELEFLEX INCORPORATEDUROLIFT — TELEFLEX INCORPORATEDUROLIFT — TELEFLEX INCORPORATEDUROLIFT — TELEFLEX INCORPORATEDUROLIFT — TELEFLEX INCORPORATEDUROLIFT — TELEFLEX INCORPORATEDUroLift — NEOTRACT, INC.UROLIFT — TELEFLEX INCORPORATEDUROLIFT — TELEFLEX INCORPORATEDUROLIFT — TELEFLEX INCORPORATEDUroLift® 2 — NEOTRACT, INC.UroLift® 2 — NEOTRACT, INC.UROLIFT — TELEFLEX INCORPORATEDUROLIFT — TELEFLEX INCORPORATEDUROLIFT — TELEFLEX INCORPORATEDUROLIFT — TELEFLEX INCORPORATEDUROLIFT — TELEFLEX INCORPORATEDUroLift® 2 — NEOTRACT, INC.UROLIFT — TELEFLEX INCORPORATEDUROLIFT — TELEFLEX INCORPORATED
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-06-24 | Neotract Inc | There is the potential that during implant deployment, the device may not properly deliver a implant. |
| 2018-07-06 | Neotract Inc | Upon implant deployment, the Capsular Tab may not be delivered as the needle is retracted. In this failure mode, the needle is deployed into the prostate and r |
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