Medical Device Manufacturer · US , Mountain View , CA

Micrus Corp. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2001

Total

Cleared

Denied

Micrus Corp. has 6 FDA 510(k) cleared medical devices. Based in Mountain View, US.

Historical record: 6 cleared submissions from 2001 to 2004. Primary specialty: Neurology.

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

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

Micrus Corp. is one of 24542 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Micrus Corp.

6 devices

1-6 of 6

Data Source

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

Last updated: Oct 06, 2026