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Avalign VM84-5161

by Avalign Technologies Inc.

Avalign VM84-5161 is a Class I device made by Avalign Technologies Inc., listed in FDA GUDID since 28 Sep 2023 (UDI-DI 00190776066147), 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 Number00190776066147 UDI-DI Date28 Sep 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  • Withdrawn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
Avalign
Generic name
Nerve/vessel retractor
Model / reference
VM84-5161
Primary DI / UDI-DI
00190776066147
FDA product code
HAO
GMDN term
Nerve/vessel retractor
Device class
Class I
Regulation number
882.4535
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Nerve/vessel retractor

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Other devices filed under Nerve/vessel retractor.

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)