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Avalign LA8277-L

by Avalign Technologies Inc.

Avalign LA8277-L is a Class II device made by Avalign Technologies Inc., listed in FDA GUDID since 23 Mar 2017 (UDI-DI 00190776001087), 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 Number00190776001087 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  • Withdrawn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
Rigid endoscopic stone-retrieval forceps, reusable
Model / reference
LA8277-L
Primary DI / UDI-DI
00190776001087
FDA product code
GEI
GMDN term
Rigid endoscopic stone-retrieval forceps, reusable
Device class
Class II
Regulation number
878.4400
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Length — 45 Centimeter
Width — 10 Millimeter

Related devices

Category: Rigid endoscopic stone-retrieval forceps, 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)