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3M™ 414-073

by 3M Unitek Corporation

3M™ 414-073 is a Class II device made by 3M Unitek Corporation, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00652221077684), 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 Number00652221077684 UDI-DI Date24 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  • Withdrawn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
3M™
Generic name
Orthodontic extraoral headgear
Model / Ref / Catalog
414-073
Primary DI / UDI-DI
00652221077684
FDA product code
DZB
GMDN term
Orthodontic extraoral headgear
Device class
Class II
Regulation number
872.5500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Orthodontic extraoral headgear

Similar devices in this category

Other devices filed under Orthodontic extraoral headgear.

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Properties

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