Skip to content

Ose 0550-010

by Orthodontic Supply & Equipment Co., Inc.

Ose 0550-010 is a Class I device made by Orthodontic Supply & Equipment Co., Inc., listed in FDA GUDID since 27 Oct 2026 (UDI-DI 00810042124882), registry data as of 9 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 9 Nov 2026.

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810042124882 UDI-DI Date27 Oct 2026ListedStatusListed 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  • Withdrawn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
0550-010
Primary DI / UDI-DI
00810042124882
FDA product code
DZC
GMDN term
Orthodontic archwire
Device class
Class I
Regulation number
872.5410
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

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

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

Properties

  • Sterilise before use
  • Single use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)