Cleared Traditional

Water-based lubricant

K253983 · Guangzhou Haoyimai Trading Co., Ltd. · Obstetrics & Gynecology
Mar 2026
Decision
84d
Days
Class 2
Risk

About This 510(k) Submission

K253983 is an FDA 510(k) clearance for the Water-based lubricant, a Lubricant, Personal (Class II — Special Controls, product code NUC), submitted by Guangzhou Haoyimai Trading Co., Ltd. (Guangzhou, CN). The FDA issued a Cleared decision on March 6, 2026, 84 days after receiving the submission on December 12, 2025. This device falls under the Obstetrics & Gynecology review panel. Regulated under 21 CFR 884.5300.

Submission Details

510(k) Number K253983 FDA.gov
FDA Decision Cleared SESE
Date Received December 12, 2025
Decision Date March 06, 2026
Days to Decision 84 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.

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