Pulsaderm, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pulsaderm, LLC - FDA 510(k) Cleared Devices
Recent clearances: Hair Laser Headband
3
Total
3
Cleared
0
Denied
Pulsaderm, LLC has 3 FDA 510(k) cleared medical devices. Based in Fort Myers, US.
Historical record: 3 cleared submissions from 2017 to 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Pulsaderm, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pulsaderm, LLC
3 devices