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3M™ Unitek™ 342-101

by 3M Unitek Corporation

3M™ Unitek™ 342-101 is a Class I device made by 3M Unitek Corporation, listed in FDA GUDID since 8 Dec 2022 (UDI-DI 00652221071712), 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 Number00652221071712 UDI-DI Date8 Dec 2022ListedStatusListed 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  • Withdrawn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™ Unitek™
Generic name
Orthodontic spring
Model / Ref / Catalog
342-101
Primary DI / UDI-DI
00652221071712
FDA product code
ECO
GMDN term
Orthodontic spring
Device class
Class I
Regulation number
872.5410
GUDID distribution status
In Commercial Distribution

Related devices

Category: Orthodontic spring

Other devices from 3M Unitek Corporation

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Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)