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Clear-Lock Ceramic 466-712

by Ortho Arch Company

Clear-Lock Ceramic 466-712 is a Class II device made by Ortho Arch Company, listed in FDA GUDID since 27 Jun 2023 (UDI-DI D9094667120), registry data as of 8 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 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberD9094667120 UDI-DI Date27 Jun 2023ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Clear-Lock Ceramic
Generic name
Orthodontic bracket, ceramic
Model / Ref / Catalog
466-712
Primary DI / UDI-DI
D9094667120
FDA product code
NJM
GMDN term
Orthodontic bracket, ceramic
Device class
Class II
Regulation number
872.5470
GUDID distribution status
In Commercial Distribution

Related devices

Category: Orthodontic bracket, ceramic

Other devices from Ortho Arch Company

See all devices from Ortho Arch Company →

Properties

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