Oktas is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Oktas - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Oktas has 7 FDA 510(k) cleared medical devices. Based in Ashland, US.
Historical record: 7 cleared submissions from 1994 to 1997. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Oktas Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Oktas
7 devices
Cleared
Apr 14, 1997
3 DIMENSIONAL VIDEO ENDOSCOPE
General & Plastic Surgery
83d
Cleared
Apr 14, 1997
VISTA MINI CAMERA SYSTEM
General & Plastic Surgery
73d
Cleared
Jul 19, 1996
3D SCOPE
General & Plastic Surgery
115d
Cleared
Jan 26, 1995
VIDEO ENDOSCOPE SYSTEM WITH ZOOM
General & Plastic Surgery
38d
Cleared
Nov 30, 1994
OKTAS STEREO VIEWING SYSTEM
Gastroenterology & Urology
91d
Cleared
Nov 22, 1994
OKTAS INTRA-ORAL DENTAL CAMERA
Dental
83d
Cleared
Jun 17, 1994
OKTAS ENDOSCOPY VIDEO CAMERA SYSTEM
Gastroenterology & Urology
58d