Medical Device Manufacturer · US , Dover , MA

Origami Surgical, LLC - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2013

Total

Cleared

Denied

Origami Surgical, LLC has 3 FDA 510(k) cleared medical devices. Based in Dover, US.

Historical record: 3 cleared submissions from 2013 to 2018. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) Regulatory Record - Origami Surgical, LLC

3 devices

1-3 of 3