FDA Device Intelligence
HomeFENTEX medical GmbH › FENTEX

FENTEX

FENTEX medical GmbH · Model 102618FX · UDI-DI 04250407709136

KAL Prescription
5
510(k) clearances
15
Adverse events
1
Recalls
123
Facilities

Description

Retractor by Fisch blunt, average opening 16.5 cm, 3 x 3 prongs

Recalls

DateFirmReason
2023-05-25TELEFLEX LLCThere are incomplete pre-cleaning instructions within the Instructions for Use (IFU).

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 docs
Data 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.