Medical Device Manufacturer · US , North Reading , MA

General Project S.R.L. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2005

Total

Cleared

Denied

General Project S.R.L. has 5 FDA 510(k) cleared medical devices. Based in North Reading, US.

Historical record: 5 cleared submissions from 2005 to 2016. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by General Project S.R.L. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by O'Connell Regulatory Consultants, Inc. as regulatory consultant.

General Project S.R.L. is one of 19087 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - General Project S.R.L.

5 devices

1-5 of 5

Data Source

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

Last updated: Sep 24, 2026