SKIA-Head (Model: SKIA-ST00)
Feb 2026
129d
Skia, Inc.
1
Total
1
Cleared
0
Denied
Skia, Inc. — FDA 510(k) Submissions
Skia, Inc. has submitted 1 FDA 510(k) premarket notifications since 2026, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include System, Image Processing, Radiological . Use the specialty filter in the sidebar to narrow results.
1 devices