Solace Therapeutics, Inc. is one of 15062 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Solace Therapeutics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Vesair 0 degree Cystoscope, Vesair 30 degree Long Cystoscope, Vesair 70 degree Long Cystoscope,Vesair 30 degree Cystoscope,Vesair 70 degree Cystoscope
1
Total
1
Cleared
0
Denied
Solace Therapeutics, Inc. has 1 FDA 510(k) cleared medical devices. Based in Farmingham, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Solace Therapeutics, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Solace Therapeutics as regulatory consultant.
FDA 510(k) Regulatory Record - Solace Therapeutics, Inc.
1 devices