Medical Device Manufacturer · US , San Juan Capistrano , CA

Neomedix Corp. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2003

Total

Cleared

Denied

Neomedix Corp. has 4 FDA 510(k) cleared medical devices. Based in San Juan Capistrano, US.

Historical record: 4 cleared submissions from 2003 to 2006. Primary specialty: General & Plastic Surgery.

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

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

Neomedix Corp. is one of 24544 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Neomedix Corp.

4 devices

1-4 of 4

Data Source

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

Last updated: Sep 28, 2026