Optik - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Optik has 6 FDA 510(k) cleared medical devices. Based in Criftib, US.
Historical record: 6 cleared submissions from 1989 to 1994. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Optik Filter by specialty or product code using the sidebar.
6 devices
Cleared
Mar 16, 1994
OPTIK LAPAROSCOPE
General & Plastic Surgery
225d
Cleared
Jun 01, 1993
COAST VIDEO ENDOSCOPIC IMAGING SYSTEM
General & Plastic Surgery
175d
Cleared
Apr 16, 1990
TITAMED ANTWERP SYSTEM
Dental
160d
Cleared
Dec 27, 1989
MANUAL SURGICAL INSTRUMENTS FOR TITAMED ANTWERP
General & Plastic Surgery
36d
Cleared
Aug 07, 1989
LIGHTSCOPE SET
Neurology
18d
Cleared
Aug 07, 1989
MINI LIGHTSCOPE SET, LIGHTSCOPE JR. SET
Orthopedic
18d