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Millennium 92-CM0128

by Avalign Technologies Inc.

Millennium 92-CM0128 is a Class I device made by Avalign Technologies Inc., listed in FDA GUDID since 12 Dec 2022 (UDI-DI 00190776298951), 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 Number00190776298951 UDI-DI Date12 Dec 2022ListedStatusListed 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  • Withdrawn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
Corneal marker, reusable
Model / reference
92-CM0128
Primary DI / UDI-DI
00190776298951
FDA product code
HMR
GMDN term
Corneal marker, reusable
Device class
Class I
Regulation number
886.4570
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Corneal marker, reusable

Similar devices in this category

Other devices filed under Corneal marker, 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)