Medical Device Manufacturer · US , Minneapolis , MN

Mr Instruments, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2004

Total

Cleared

Denied

Mr Instruments, Inc. has 7 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Historical record: 7 cleared submissions from 2004 to 2017. Primary specialty: Radiology.

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

510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.

Mr Instruments, Inc. is one of 13688 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Mr Instruments, Inc.

7 devices

1-7 of 7

Data Source

Sourced from the FDA 510(k) public files . 175,972 total devices indexed.

Last updated: Sep 14, 2026