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Ose 0271-Dc

by Orthodontic Supply & Equipment Co., Inc.

Ose 0271-Dc is a Class I device made by Orthodontic Supply & Equipment Co., Inc., listed in FDA GUDID since 29 Apr 2020 (UDI-DI 00810042123007), 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 Number00810042123007 UDI-DI Date29 Apr 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  • Withdrawn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
0271-DC
Primary DI / UDI-DI
00810042123007
FDA product code
ECN
GMDN term
Orthodontic archwire
Device class
Class I
Regulation number
872.5410
GUDID distribution status
In Commercial Distribution

Related devices

Category: Orthodontic archwire

Similar devices in this category

Other devices filed under 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)