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Facebow 617-1013

by Ormco Corporation

Facebow 617-1013 is a Class II device made by Ormco Corporation, listed in FDA GUDID since 8 Sep 2016 (UDI-DI 00889989079852), 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 Number00889989079852 UDI-DI Date8 Sep 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  • Withdrawn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
Facebow
Generic name
Orthodontic face bow
Model / reference
617-1013
Description
Facebow ,SHRT OB,STD MED IB, 045
Primary DI / UDI-DI
00889989079852
FDA product code
DZB
GMDN term
Orthodontic face bow
Device class
Class II
Regulation number
872.5500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Orthodontic face bow

Other devices from Ormco Corporation

See all devices from Ormco Corporation →

Properties

  • Single use
  • Prescription use
  • Lot / batch number
Other properties (12, all answered No)