Medical Device Manufacturer · US , Natick , MA

Neothermia Corp. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2001

Total

Cleared

Denied

Neothermia Corp. has 7 FDA 510(k) cleared medical devices. Based in Natick, US.

Historical record: 7 cleared submissions from 2001 to 2004. Primary specialty: General & Plastic Surgery.

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

Neothermia Corp. 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 - Neothermia Corp.

7 devices

1-7 of 7