Oki Shiks USA , Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Oki Shiks USA , Ltd. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Oki Shiks USA , Ltd. has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 9 cleared submissions from 1980 to 1982. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Oki Shiks USA , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Oki Shiks USA , Ltd.
9 devices
Cleared
Jun 07, 1982
REIGNING DENTURE
Dental
41d
Cleared
Nov 19, 1980
REIGNING DENTURE
Dental
40d
Cleared
Nov 12, 1980
REIGNING CROWN BRIDGE
Dental
33d
Cleared
Nov 12, 1980
REIGNING REPAIR EPOXY RESIN
Dental
33d
Cleared
Nov 12, 1980
REIGNING ARTIFICIAL TEETH
Dental
33d
Cleared
Jul 08, 1980
REIGNING EPOXY RESIN CEMENT
Dental
42d
Cleared
Jun 20, 1980
REIGNING ARTIFICIAL TEETH/POLYCARB.RESIN
Dental
24d
Cleared
Jun 09, 1980
REIGNING DENTURE MADE OF POLYCARB. RESIN
Dental
13d
Cleared
Jun 09, 1980
REIGNING CROWN-BRIDGE/POLYCARB. RESIN
Dental
13d