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Damon 3 491-4721

by Ormco Corporation

Damon 3 491-4721 is a Class II device made by Ormco Corporation, listed in FDA GUDID since 8 Sep 2016 (UDI-DI 00889989003642), registry data as of 22 Oct 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00889989003642 UDI-DI Date8 Sep 2016ListedStatusListed 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  • Withdrawn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
Damon 3
Generic name
Orthodontic bracket, plastic, single-use
Model / reference
491-4721
Primary DI / UDI-DI
00889989003642
FDA product code
DYW
GMDN term
Orthodontic bracket, plastic, single-use
Device class
Class II
Regulation number
872.5470
GUDID distribution status
In Commercial Distribution

Related devices

Category: Orthodontic bracket, plastic, single-use

Other devices from Ormco Corporation

See all devices from Ormco Corporation →

Properties

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