Medical Device Manufacturer · US , Somerset , MA

Inolase 2002, Ltd. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2006

Total

Cleared

Denied

Inolase 2002, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Somerset, US.

Historical record: 2 cleared submissions from 2006 to 2007. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Inolase 2002, Ltd. Filter by specialty or product code using the sidebar.

Inolase 2002, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Inolase 2002, Ltd.

2 devices

1-2 of 2