Wellspring Pharmaceutical Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Wellspring Pharmaceutical Corporation - FDA 510(k) Cleared Devices
Recent clearances: Bonine Acupressure Bands
1
Total
1
Cleared
0
Denied
Wellspring Pharmaceutical Corporation has 1 FDA 510(k) cleared medical devices. Based in Sarasota, US.
Last cleared in 2021. Active since 2021. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Wellspring Pharmaceutical Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Drug Device Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Wellspring Pharmaceutical Corporation
1 devices