Medical Device Manufacturer · US , Framingham , MA

Interlace Medical, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2008

Total

Cleared

Denied

Interlace Medical, Inc. has 7 FDA 510(k) cleared medical devices. Based in Framingham, US.

Historical record: 7 cleared submissions from 2008 to 2011. Primary specialty: Obstetrics & Gynecology.

Browse the FDA 510(k) cleared devices submitted by Interlace Medical, Inc. Filter by specialty or product code using the sidebar.

Interlace Medical, Inc. 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 - Interlace Medical, Inc.

7 devices

1-7 of 7