Medical Device Manufacturer · US , Santa Clara , CA

Nitto Denko America, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1985

Total

Cleared

Denied

Nitto Denko America, Inc. has 5 FDA 510(k) cleared medical devices. Based in Santa Clara, US.

Historical record: 5 cleared submissions from 1985 to 1987. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Nitto Denko America, Inc. Filter by specialty or product code using the sidebar.

Nitto Denko America, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Nitto Denko America, Inc.

5 devices

1-5 of 5