Medical Device Manufacturer · US , New York , NY

Kuraray Company, Ltd. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1994

Recent clearances: CLEARFIL DC CEMENT, TEETHMATE F-1

Total

Cleared

Denied

Kuraray Company, Ltd. has 10 FDA 510(k) cleared dental devices. Based in New York, US.

Historical record: 10 cleared submissions from 1994 to 2000.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

Kuraray Company, Ltd. is one of 7469 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Kuraray Company, Ltd.

10 devices

1-10 of 10

CLEARFIL LINER BOND SYSTEM

CLEARFIL AP-X AND LINER BOND 2

K943169 · EBF

Dental · 40d

Cleared Aug 10, 1994

CLEARFIL LINER BOND 2

K943170 · KLE

Dental · 40d

Kuraray Company, Ltd. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Kuraray Company, Ltd.

Filters