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Fibernex LF0101X940

by Typenex Medical, LLC

Fibernex LF0101X940 is a Class II device made by Typenex Medical, LLC, listed in FDA GUDID since 27 Dec 2016 (UDI-DI B050LF0101X9400), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberB050LF0101X9400 UDI-DI Date27 Dec 2016ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Fibernex
Generic name
Laser lithotripsy system
Model / reference
LF0101X940
Primary DI / UDI-DI
B050LF0101X9400
FDA product code
GEX
GMDN term
Laser lithotripsy system
Device class
Class II
Regulation number
878.4810
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — 940 Micrometer

Related devices

Category: Laser lithotripsy system

Similar devices

Other devices filed under FDA product code GEX (Powered Laser Surgical Instrument).

Other devices from Typenex Medical, LLC

See all devices from Typenex Medical, LLC →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)