Medical Device Manufacturer · US , Lake Forest , CA

Monobind, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2008

Total

Cleared

Denied

Monobind, Inc. has 2 FDA 510(k) cleared medical devices. Based in Lake Forest, US.

Historical record: 2 cleared submissions from 2008 to 2018. Primary specialty: Chemistry.

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

FDA 510(k) Regulatory Record - Monobind, Inc.

2 devices

1-2 of 2