The Kama Sutra Company is one of 21998 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
The Kama Sutra Company - FDA 510(k) Cleared Devices
Recent clearances: Love Liquid Personal Lubricant
1
Total
1
Cleared
0
Denied
The Kama Sutra Company has 1 FDA 510(k) cleared medical devices. Based in Thousand Oaks, US.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by The Kama Sutra Company Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Med-Device Consulting, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - The Kama Sutra Company
1 devices