Medical Device Manufacturer · US , Seattle , WA

Ostex Intl., Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1995

Total

Cleared

Denied

Ostex Intl., Inc. has 5 FDA 510(k) cleared medical devices. Based in Seattle, US.

Historical record: 5 cleared submissions from 1995 to 2001. Primary specialty: Chemistry.

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

Ostex Intl., 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 - Ostex Intl., Inc.

5 devices

1-5 of 5