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Millennium 92-F2160

by Avalign Technologies Inc.

Millennium 92-F2160 is a Class I device made by Avalign Technologies Inc., listed in FDA GUDID since 17 Nov 2023 (UDI-DI 00190776308308), 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 Number00190776308308 UDI-DI Date17 Nov 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  • Withdrawn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
Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable
Model / reference
92-F2160
Primary DI / UDI-DI
00190776308308
FDA product code
HNR
GMDN term
Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable
Device class
Class I
Regulation number
886.4350
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable

Similar devices in this category

Other devices filed under Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable.

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)