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N.A. -741-0721

by Forestadent Bernhard Förster GmbH GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberEFOR74107211 UDI-DIDate24 Sep 2019ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Generic Name
Orthodontic tube
Model / Reference
-741-0721
Primary DI / UDI-DI
EFOR74107211
FDA Product Code
DZD
GMDN Term
Orthodontic tube
Device Class
Class I
Regulation Number
872.5410
GUDID distribution status
In Commercial Distribution

Related devices

Category: Orthodontic tube

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 (9)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No