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179M0718-010

by Forestadent Bernhard Förster GmbH

179M0718-010 (-179M0718-010) is a Class I device made by Forestadent Bernhard Förster GmbH, listed in FDA GUDID since 2 Oct 2019 (UDI-DI EFOR179M07180101), 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 NumberEFOR179M07180101 UDI-DI Date2 Oct 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  • Withdrawn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 appliance system, bonded
Model / reference
-179M0718-010
Primary DI / UDI-DI
EFOR179M07180101
FDA product code
DYJ
GMDN term
Orthodontic appliance system, bonded
Device class
Class I
Regulation number
872.5410
GUDID distribution status
In Commercial Distribution

Related devices

Category: Orthodontic appliance system, bonded

Similar devices

Other devices filed under FDA product code DYJ (RETAINER, SCREW EXPANSION, ORTHODONTIC).

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)