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Frida 05001401

by Fridababy, LLC

Frida 05001401 is a Class II device made by Fridababy, LLC, listed in FDA GUDID since 2 Jul 2025 (UDI-DI 00810028770508), 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 Number00810028770508 UDI-DI Date2 Jul 2025ListedStatusListed 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  • Withdrawn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
Frida
Generic name
Teething device, fluid-filled
Model / reference
05001401
Primary DI / UDI-DI
00810028770508
FDA product code
KKO
GMDN term
Teething device, fluid-filled
Device class
Class II
Regulation number
872.5550
GUDID distribution status
In Commercial Distribution

Related devices

Category: Teething device, fluid-filled

Similar devices

Also classified as Teething device, fluid-filled.

Similar devices

Other devices filed under FDA product code KKO (Ring, Teething, Fluid-Filled).

Other devices from Fridababy, LLC

See all devices from Fridababy, LLC →

Properties

  • Over-the-counter
  • Premarket exempt
Other properties (13, all answered No)