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Ose 4999-544A

by Orthodontic Supply & Equipment Co., Inc.

Ose 4999-544A is a Class I device made by Orthodontic Supply & Equipment Co., Inc., listed in FDA GUDID since 4 May 2020 (UDI-DI 00810042123922), 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 Number00810042123922 UDI-DI Date4 May 2020ListedStatusListed 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  • Withdrawn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
Ose
Generic name
Orthodontic archwire
Model / reference
4999-544A
Primary DI / UDI-DI
00810042123922
FDA product code
DZC
GMDN term
Orthodontic archwire
Device class
Class I
Regulation number
872.5410
GUDID distribution status
In Commercial Distribution

Related devices

Category: Orthodontic archwire

Other devices from Orthodontic Supply & Equipment Co., Inc.

See all devices from Orthodontic Supply & Equipment Co., Inc. →

Properties

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