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FENTEX

FENTEX medical GmbH · Model 102817FX · UDI-DI 04250407709198

KAL Prescription
5
510(k) clearances
15
Adverse events
1
Recalls
124
Facilities

Description

Retractor by Fisch 16.5 cm, 2 pr. left, solid blade right

Recalls

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

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.