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Avalign VM107-9141

by Avalign Technologies Inc.

Avalign VM107-9141 is a Class I device made by Avalign Technologies Inc., listed in FDA GUDID since 28 Sep 2023 (UDI-DI 00190776231446), 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 Number00190776231446 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  • Withdrawn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
Endaural surgical curette, reusable
Model / reference
VM107-9141
Primary DI / UDI-DI
00190776231446
FDA product code
JYG
GMDN term
Endaural surgical curette, 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: Endaural surgical curette, reusable

Similar devices in this category

Other devices filed under Endaural surgical curette, 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)