Theyfit is one of 22097 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Theyfit - FDA 510(k) Cleared Devices
Recent clearances: TheyFit Male Condom, THEYFIT MALE CONDOM
2
Total
2
Cleared
0
Denied
Theyfit has 2 FDA 510(k) cleared medical devices. Based in Swanee, US.
Historical record: 2 cleared submissions from 2013 to 2015. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Theyfit Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regsoultions, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Theyfit
2 devices