Osko, Inc. is one of 13011 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Osko, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Edge Air(1417) Digital Flat Panel X-ray Detector, Edge Air Digital Flat Panel X-ray Detector, Edge Digital Flat Panel X-ray Detector
6
Total
6
Cleared
0
Denied
Osko, Inc. has 6 FDA 510(k) cleared medical devices. Based in Miami, US.
Historical record: 6 cleared submissions from 2015 to 2020. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Osko, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mtechgroup as regulatory consultant.
FDA 510(k) Regulatory Record - Osko, Inc.
6 devices
Cleared
Jun 29, 2020
Edge Air(1417) Digital Flat Panel X-ray Detector
Radiology
24d
Cleared
Oct 06, 2017
Edge Air Digital Flat Panel X-ray Detector
Radiology
30d
Cleared
Oct 06, 2017
Edge Digital Flat Panel X-ray Detector
Radiology
30d
Cleared
Jul 28, 2017
Smart Stitching Software System, Image Processing, Radiological
Radiology
269d
Cleared
May 07, 2015
Diagnostic X-ray System
Radiology
52d
Cleared
Apr 08, 2015
ELIAN Digital Diagnostic X-ray System
Radiology
41d