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Avalign VM101-5676

by Avalign Technologies Inc.

Avalign VM101-5676 is a Class I device made by Avalign Technologies Inc., listed in FDA GUDID since 3 Nov 2021 (UDI-DI 00190776043223), 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 Number00190776043223 UDI-DI Date3 Nov 2021ListedStatusListed 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  • Withdrawn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
Avalign
Generic name
Ear scissors, reusable
Model / reference
VM101-5676
Primary DI / UDI-DI
00190776043223
FDA product code
JZB
GMDN term
Ear scissors, reusable
Device class
Class I
Regulation number
874.4420
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Ear scissors, reusable

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Other devices filed under Ear scissors, reusable.

Other devices from Avalign Technologies Inc.

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Properties

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