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Tentacle Teether Tentacle Violet 3.0

by Casco Bay Molding

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00860012961009 UDI-DI Date24 Nov 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Tentacle Teether
Generic Name
Teething device, non-fluid-filled
Model / Reference
Tentacle Violet 3.0
Primary DI / UDI-DI
00860012961009
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

Other devices from Casco Bay Molding

See all devices from Casco Bay Molding →

Properties

  • Premarket Exempt
  • Lot / Batch Number

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No