Fulwell, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Fulwell, LLC - FDA 510(k) Cleared Devices
Recent clearances: RF Surgical Generator, Electrosurgical Generator
2
Total
2
Cleared
0
Denied
Fulwell, LLC has 2 FDA 510(k) cleared medical devices. Based in Miami, US.
Historical record: 2 cleared submissions from 2019 to 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Fulwell, LLC Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Guangzhou Keda Testing Tech Co., Ltd. and Guangzhou Keda Biological Tech Co., Ltd..
FDA 510(k) Regulatory Record - Fulwell, LLC
2 devices