Cleared Traditional

K212260 - Sensuva Premium Silicone Personal Lubricant (FDA 510(k) Clearance)

Apr 2022
Decision
267d
Days
Class 2
Risk

K212260 is an FDA 510(k) clearance for the Sensuva Premium Silicone Personal Lubricant. This device is classified as a Lubricant, Personal (Class II - Special Controls, product code NUC).

Submitted by Valencia Naturals, Inc. (Chatsworth, US). The FDA issued a Cleared decision on April 13, 2022, 267 days after receiving the submission on July 20, 2021.

This device falls under the Obstetrics & Gynecology FDA review panel. Regulated under 21 CFR 884.5300. This Device Is A Personal Lubricant, For Penile And/or Vaginal Application, Intended To Moisturize And Lubricate, To Enhance The Ease And Comfort Of Intimate Sexual Activity, And Supplement The Body's Natural Lubrication. This Product May Or May Not Be Compatible With Natural Rubber Latex, Polyisoprene, And/or Polyurethane Condoms..

Submission Details

510(k) Number K212260 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 20, 2021
Decision Date April 13, 2022
Days to Decision 267 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary Summary PDF

Device Classification

Product Code NUC - Lubricant, Personal
Device Class Class II - Special Controls
CFR Regulation 21 CFR 884.5300
Definition This Device Is A Personal Lubricant, For Penile And/or Vaginal Application, Intended To Moisturize And Lubricate, To Enhance The Ease And Comfort Of Intimate Sexual Activity, And Supplement The Body's Natural Lubrication. This Product May Or May Not Be Compatible With Natural Rubber Latex, Polyisoprene, And/or Polyurethane Condoms.