Fentex 428501FX

by FENTEX medical GmbH

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number04250407734947 UDI-DI	Date12 Dec 2022Listed	StatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Fentex
Generic Name: Surgical retractor/retraction system blade, reusable
Model / Ref / Catalog: 428501FX
Description: Tongue Depressor by Davis-Meyer size 1, 29 x 70 mm

Primary DI / UDI-DI: 04250407734947
FDA Product Code: LRC
GMDN Term: Surgical retractor/retraction system blade, reusable

Device Class: Class I
Regulation Number: 874.4420
GUDID distribution status: Not in Commercial Distribution

Sterilization Method: Moist Heat or Steam Sterilization

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See all devices from FENTEX medical GmbH →

Properties

Prescription Use
Premarket Exempt
Lot / Batch Number

Other properties (11)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Serial Number: No
Expiration Date: No
Manufacturing Date: No