Medical Device Manufacturer · US , Los Angeles , CA

Medrange Corporation - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2010

Total

Cleared

Denied

Medrange Corporation has 2 FDA 510(k) cleared medical devices. Based in Los Angeles, US.

Historical record: 2 cleared submissions from 2010 to 2012. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Medrange Corporation Filter by specialty or product code using the sidebar.

Medrange Corporation 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 - Medrange Corporation

2 devices

1-2 of 2