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Ose 0132-004

by Orthodontic Supply & Equipment Co., Inc.

Ose 0132-004 is a Class II device made by Orthodontic Supply & Equipment Co., Inc., listed in FDA GUDID since 29 Jul 2016 (UDI-DI 00869843000253), 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 Number00869843000253 UDI-DI Date29 Jul 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  • Withdrawn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
Ose
Generic name
Glass ionomer dental cement
Model / reference
0132-004
Primary DI / UDI-DI
00869843000253
FDA product code
EMA
GMDN term
Glass ionomer dental cement
Device class
Class II
Regulation number
872.3275
GUDID distribution status
In Commercial Distribution

Related devices

Category: Glass ionomer dental cement

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

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

Properties

  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)