Cleared Traditional

K150072 - TheyFit Male Condom

K150072 is an FDA 510(k) clearance for TheyFit Male Condom, manufactured by Theyfit. The device is a Class 2 Obstetrics & Gynecology device with product code HIS cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K150072 · Theyfit · Obstetrics & Gynecology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Apr 2015
Decision
90d
Days
Class 2
Risk

K150072 is an FDA 510(k) clearance for the TheyFit Male Condom. Classified as Condom (product code HIS), Class II - Special Controls.

Submitted by Theyfit (Covington, US). The FDA issued a Cleared decision on April 14, 2015 after a review of 90 days - within the typical 510(k) review window.

This device falls under the Obstetrics & Gynecology FDA review panel, regulated under 21 CFR 884.5300 - the FDA obstetrics and gynecology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Obstetrics & Gynecology review framework, consistent with the majority of Class II 510(k) submissions.

View all Theyfit devices

FDA 510(k) Submission Details - K150072

510(k) Number K150072 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 14, 2015
Decision Date April 14, 2015
Days to Decision 90 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
70d faster than avg
Panel avg: 160d · This submission: 90d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HIS Device Classification - Class 2, Special Controls

Product Code HIS Condom
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 884.5300
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Obstetrics & Gynecology devices follow this clearance model.

Regulatory Peers - HIS Condom

All 76
Devices cleared under the same product code (HIS) and FDA review panel - the closest regulatory comparables to K150072.
Lifestyles Zero Lubricated Latex Male Condom
K163107 · Ansell Healthcare Products, LLC · Jan 2017
Trojan XOXO Ribbed Male Natural Rubber Latex Condom with Silicone and Aloe Lubricant
K161915 · Church & Dwight Co., Inc. · Sep 2016
Trojan XOXO Thin Male Natural Rubber Latex Condom with Silicone and Aloe Lubricant
K161545 · Church & Dwight Co., Inc. · Aug 2016
TROJAN JAGUAR MALE NATURAL RUBBER LATEX CONDOM WITH WARMING AND TINGLING LUBRICANT
K131887 · Church & Dwight Co., Inc. · Oct 2013
TROJAN HER PLEASURE (RIBBED) ECSTASY LATEX CONDOM WITH LUBRICANT
K120286 · Church & Dwight Co., Inc. · Jun 2012
TROJAN MAGNUM CONDOM WITH FIRE & ICE LUBRICANT
K120287 · Church & Dwight Co., Inc. · May 2012