Trigg Laboratories Dba Wet International is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Trigg Laboratories Dba Wet International - FDA 510(k) Cleared Devices
Recent clearances: Wet Organics Personal Lubricant
1
Total
1
Cleared
0
Denied
Trigg Laboratories Dba Wet International has 1 FDA 510(k) cleared medical devices. Based in Las Vegas, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Trigg Laboratories Dba Wet International 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 - Trigg Laboratories Dba Wet International
1 devices