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Sassy 81031R1FC

by Sassy Baby, Inc.

Sassy 81031R1FC is a Class II device made by Sassy Baby, Inc., listed in FDA GUDID since 21 May 2026 (UDI-DI 00037977810318), registry data as of 8 Nov 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 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00037977810318 UDI-DI Date21 May 2026ListedStatusListed 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  • Withdrawn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
Sassy
Generic name
Teething device, fluid-filled
Model / reference
81031R1FC
Primary DI / UDI-DI
00037977810318
FDA product code
KKO
GMDN term
Teething device, fluid-filled
Device class
Class II
Regulation number
872.5550
GUDID distribution status
In Commercial Distribution

Similar devices

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

Other devices from Sassy Baby, Inc.

See all devices from Sassy Baby, Inc. →

Properties

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