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Dr. Brown's TE026

by Dr. Brown's Company

Dr. Brown's TE026 is a Class I device made by Dr. Brown's Company, listed in FDA GUDID since 30 Nov 2022 (UDI-DI 00072239326442), 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 Number00072239326442 UDI-DI Date30 Nov 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  • Withdrawn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
Dr. Brown's
Generic name
Teething device, non-fluid-filled
Model / reference
TE026
Primary DI / UDI-DI
00072239326442
FDA product code
MEF
GMDN term
Teething device, non-fluid-filled
Device class
Class I
Regulation number
872.5550
GUDID distribution status
In Commercial Distribution

Related devices

Category: Infant care kit

Other devices from Dr. Brown's Company

See all devices from Dr. Brown's Company →

Properties

  • Premarket exempt
  • Lot / batch number
Other properties (13, all answered No)