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Vera Bradley VB Tilly Superbloom

by Mcgee Group, Inc., the

Vera Bradley VB Tilly Superbloom (VBTILLY0SBM0OPT) is a Class II device made by Mcgee Group, Inc., the, listed in FDA GUDID since 25 Oct 2019 (UDI-DI 00781096546145), 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 Number00781096546145 UDI-DI Date25 Oct 2019ListedStatusListed 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  • Withdrawn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
Vera Bradley
Generic name
Spectacle frame
Model / Ref / Catalog
VB Tilly Superbloom, VBTILLY0SBM0OPT
Primary DI / UDI-DI
00781096546145
FDA product code
HQR
GMDN term
Spectacle frame
Device class
Class II
Regulation number
886.4100
GUDID distribution status
In Commercial Distribution

Related devices

Category: Spectacle frame

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Properties

  • Over-the-counter
  • Premarket exempt
Other properties (13, all answered No)