Medical Device Manufacturer · US , West Cadwell , NJ

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

6 submissions · 6 cleared · Since 2004

Total

Cleared

Denied

Takara Belmont USA, Inc. has 6 FDA 510(k) cleared medical devices. Based in West Cadwell, US.

Historical record: 6 cleared submissions from 2004 to 2011. Primary specialty: Radiology.

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

510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.

Takara Belmont USA, Inc. is one of 20464 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Takara Belmont USA, Inc.

6 devices

1-6 of 6

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Sep 25, 2026