Medical Device Manufacturer · US , Scottsdale , AZ

Topera, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2011

Total

Cleared

Denied

Topera, Inc. has 7 FDA 510(k) cleared medical devices. Based in Scottsdale, US.

Historical record: 7 cleared submissions from 2011 to 2015. Primary specialty: Cardiovascular.

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

Topera, Inc. is one of 5032 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Topera, Inc.

7 devices

1-7 of 7