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Avalign VM84-2256

by Avalign Technologies Inc.

Avalign VM84-2256 is a Class II device made by Avalign Technologies Inc., listed in FDA GUDID since 23 Mar 2017 (UDI-DI 00190776015527), 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 Number00190776015527 UDI-DI Date23 Mar 2017ListedStatusListed 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  • Withdrawn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
Self-retaining surgical retractor, reusable
Model / reference
VM84-2256
Primary DI / UDI-DI
00190776015527
FDA product code
GZT
GMDN term
Self-retaining surgical retractor, reusable
Device class
Class II
Regulation number
882.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Length — 6 Inch
Width — 20 Millimeter
Length — 60 Millimeter

Related devices

Category: Self-retaining surgical retractor, reusable

Other devices from Avalign Technologies Inc.

See all devices from Avalign Technologies Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
Other properties (12, all answered No)