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Millennium 17-090499

by Avalign Technologies Inc.

Millennium 17-090499 is a Class I device made by Avalign Technologies Inc., listed in FDA GUDID since 22 Feb 2023 (UDI-DI 00190776364236), registry data as of 8 Nov 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 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00190776364236 UDI-DI Date22 Feb 2023ListedStatusListed 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  • Withdrawn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

Trade name
Millennium
Generic name
Tooth extraction forceps
Model / reference
17-090499
Primary DI / UDI-DI
00190776364236
FDA product code
EMG
GMDN term
Tooth extraction forceps
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Tooth extraction forceps

Similar devices

Other devices filed under FDA product code EMG (FORCEPS, TOOTH EXTRACTOR, SURGICAL).

Other devices from Avalign Technologies Inc.

See all devices from Avalign Technologies Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)