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Alflbl

by Flexmedics

Alflbl is a Class II device made by Flexmedics, listed in FDA GUDID since 27 May 2020 (UDI-DI 10195291007542), 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 Number10195291007542 UDI-DI Date27 May 2020ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Generic name
Alginate dental impression material
Model / reference
ALFLBL
Primary DI / UDI-DI
10195291007542
FDA product code
ELW
GMDN term
Alginate dental impression material
Device class
Class II
Regulation number
872.3660
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code ELW (Material, Impression).

Other devices from Flexmedics

See all devices from Flexmedics →

Properties

  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (11, all answered No)