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Quickie Kit Quickie Kit - Deep Anal - White

by Blush Novelties

Quickie Kit Quickie Kit - Deep Anal - White (BL-50154) is a Class II device made by Blush Novelties, listed in FDA GUDID since 29 Oct 2019 (UDI-DI 00853858007673), 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 Number00853858007673 UDI-DI Date29 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  • Withdrawn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
Quickie Kit
Generic name
Penile ring
Model / Ref / Catalog
Quickie Kit - Deep Anal - White, BL-50154
Primary DI / UDI-DI
00853858007673
FDA product code
LKY
GMDN term
Penile ring
Device class
Class II
Regulation number
876.5020
GUDID distribution status
In Commercial Distribution

Related devices

Category: Penile ring

Similar devices

Other devices filed under FDA product code LKY (Device, External Penile Rigidity).

Other devices from Blush Novelties

See all devices from Blush Novelties →

Properties

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