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Nuby 6921

by Luv N' Care, Ltd.

Nuby 6921 is a Class II device made by Luv N' Care, Ltd., listed in FDA GUDID since 23 Oct 2020 (UDI-DI 00048526069217), 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 Number00048526069217 UDI-DI Date23 Oct 2020ListedStatusListed 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  • Withdrawn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
Nuby
Generic name
Teething device, fluid-filled
Model / reference
6921
Primary DI / UDI-DI
00048526069217
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

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

Other devices from Luv N' Care, Ltd.

See all devices from Luv N' Care, Ltd. →

Properties

  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)