Origami Surgical, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Origami Surgical, LLC - FDA 510(k) Cleared Devices
Recent clearances: StitchKit V-Loc 90, StitchKit V-Loc 180, StitchKit Quill PDO
3
Total
3
Cleared
0
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.
510(k) submissions have been managed by Clover Medical, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Origami Surgical, LLC
3 devices