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Ose 0202-G

by Orthodontic Supply & Equipment Co., Inc.

Ose 0202-G is a Class I device made by Orthodontic Supply & Equipment Co., Inc., listed in FDA GUDID since 21 Jun 2023 (UDI-DI 00810042124554), 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 Number00810042124554 UDI-DI Date21 Jun 2023ListedStatusListed 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  • Withdrawn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
Self-retaining surgical retractor, reusable
Model / reference
0202-G
Primary DI / UDI-DI
00810042124554
FDA product code
EIF
GMDN term
Self-retaining surgical retractor, reusable
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution
Sterilisation method
Liquid Chemical

Related devices

Category: Self-retaining surgical retractor, reusable

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

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

Properties

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