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Avalign VM81-1062C20

by Avalign Technologies Inc.

Avalign VM81-1062C20 is a Class II device made by Avalign Technologies Inc., listed in FDA GUDID since 23 Mar 2017 (UDI-DI 00190776011659), 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 Number00190776011659 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  • Withdrawn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
Spinal rongeur
Model / reference
VM81-1062C20
Primary DI / UDI-DI
00190776011659
FDA product code
HAE
GMDN term
Spinal rongeur
Device class
Class II
Regulation number
882.4840
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Width — 3 Millimeter
Length — 8 Inch
Angle — 40 degree

Related devices

Category: Spinal rongeur

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)