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Opulent Global 777

by Casco Bay Molding

Opulent Global 777 is a Class I device made by Casco Bay Molding, listed in FDA GUDID since 27 Apr 2022 (UDI-DI 00860006862718), 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 Number00860006862718 UDI-DI Date27 Apr 2022ListedStatusListed 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  • Withdrawn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
Opulent Global
Generic name
Teething device, non-fluid-filled
Model / reference
777
Primary DI / UDI-DI
00860006862718
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

Related devices

Category: Teething device, non-fluid-filled

Other devices from Casco Bay Molding

See all devices from Casco Bay Molding →

Properties

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