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Performance Plus - Flex Pro - Blue

by Blush Novelties

Performance Plus - Flex Pro - Blue (BL-90002) is a Class II device made by Blush Novelties, listed in FDA GUDID since 17 Mar 2025 (UDI-DI 00850002870718), 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 Number00850002870718 UDI-DI Date17 Mar 2025ListedStatusListed 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  • Withdrawn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
Performance Plus
Generic name
Penile ring
Model / Ref / Catalog
Performance Plus - Flex Pro - Blue, BL-90002
Primary DI / UDI-DI
00850002870718
FDA product code
LKY
GMDN term
Penile ring
Device class
Class II
Regulation number
876.5020
GUDID distribution status
In Commercial Distribution

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)