Medical Device Manufacturer · US , Park City , UT

Mitaka USA, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1999

Total

Cleared

Denied

Mitaka USA, Inc. has 2 FDA 510(k) cleared medical devices. Based in Park City, US.

Historical record: 2 cleared submissions from 1999 to 1999. Primary specialty: General & Plastic Surgery.

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

Mitaka USA, 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 - Mitaka USA, Inc.

2 devices

1-2 of 2