Wellquest International, Inc. is one of 18949 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Wellquest International, Inc. - FDA 510(k) Cleared Devices
Recent clearances: NuBrilliance Light Pain Therapy
1
Total
1
Cleared
0
Denied
Wellquest International, Inc. has 1 FDA 510(k) cleared medical devices. Based in New York, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Wellquest International, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Emergo Global Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Wellquest International, Inc.
1 devices