Sketchpad Innovations, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sketchpad Innovations, LLC - FDA 510(k) Cleared Devices
Recent clearances: Kava and Kava with Herbst
1
Total
1
Cleared
0
Denied
Sketchpad Innovations, LLC has 1 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Sketchpad Innovations, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Fishermed Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Sketchpad Innovations, LLC
1 devices