Inkspace Imaging, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Inkspace Imaging, Inc. - FDA 510(k) Cleared Devices
Recent clearances: InkSpace Imaging Small Body Array (SBA12PH30x), InkSpace Imaging Small Body Array, InkSpace Imaging Small Body Array
5
Total
5
Cleared
0
Denied
Inkspace Imaging, Inc. has 5 FDA 510(k) cleared medical devices. Based in Pleasanton, US.
Latest FDA clearance: Oct 2025. Active since 2021. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Inkspace Imaging, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Veranex, Inc. and Experien Group, LLC.
FDA 510(k) Regulatory Record - Inkspace Imaging, Inc.
5 devices
Cleared
Oct 20, 2025
InkSpace Imaging Small Body Array (SBA12PH30x)
Radiology
24d
Cleared
Dec 20, 2024
InkSpace Imaging Small Body Array
Radiology
23d
Cleared
Jan 08, 2024
InkSpace Imaging Small Body Array
Radiology
81d
Cleared
Dec 08, 2022
InkSpace Imaging Body Array
Radiology
17d
Cleared
Dec 17, 2021
InkSpace Imaging Pediatric Body Array
Radiology
60d