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Lovehoney Cherry 3.4oz

by Westridge Laboratories Incorporated

Lovehoney Cherry 3.4oz (IDD11350) is a Class II device made by Westridge Laboratories Incorporated, cleared under FDA 510(k) K051295 on 15 Feb 2006 and listed in FDA GUDID since 7 Apr 2023 (UDI-DI 05060493009862), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K051295

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05060493009862 UDI-DI Date7 Apr 2023ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK051295 Date15 Feb 2006DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K051295 decided 15 Feb 2006 Active
  • FDA GUDID UDI-DI 05060493009862 listed 7 Apr 2023 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K051295
  2. Listed FDA GUDID 05060493009862

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Lovehoney Cherry
Generic name
Sexual lubricant
Model / Ref / Catalog
Lovehoney Cherry 3.4oz, IDD11350
Primary DI / UDI-DI
05060493009862
510(k) Number
FDA product code
NUC
GMDN term
Sexual lubricant
Device class
Class II
Regulation number
884.5300
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code NUC (Lubricant, Personal).

Other devices from Westridge Laboratories Incorporated

See all devices from Westridge Laboratories Incorporated →

Properties

  • Contains latex
  • Over-the-counter
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)