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Ingenuity 16881

by Kids II, Inc.

Ingenuity 16881 is a Class II device made by Kids II, Inc., listed in FDA GUDID since 28 Apr 2023 (UDI-DI 00074451168817), 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 Number00074451168817 UDI-DI Date28 Apr 2023ListedStatusListed 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  • Withdrawn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
Ingenuity
Generic name
Teething device, fluid-filled
Model / reference
16881
Primary DI / UDI-DI
00074451168817
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 Kids II, Inc.

See all devices from Kids II, Inc. →

Properties

  • Premarket exempt
Other properties (14, all answered No)