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606-0130

by Forestadent Bernhard Förster GmbH

606-0130 (-606-0130) is a Class II device made by Forestadent Bernhard Förster GmbH, listed in FDA GUDID since 24 Sep 2019 (UDI-DI EFOR60601301), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberEFOR60601301 UDI-DI Date24 Sep 2019ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Generic name
Orthodontic face bow
Model / reference
-606-0130
Primary DI / UDI-DI
EFOR60601301
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 Forestadent Bernhard Förster GmbH

See all devices from Forestadent Bernhard Förster GmbH →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)