Medical Device Manufacturer · US , Madison , NJ

Origami Surgical

2 submissions · 2 cleared · Since 2019
2
Total
2
Cleared
0
Denied

Origami Surgical — FDA 510(k) Submissions

Origami Surgical has submitted 2 FDA 510(k) premarket notifications since 2019, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Suture, Surgical, Nonabsorbable, Expanded, Polytetraflouroethylene, Suture, Absorbable, Synthetic, Polyglycolic Acid . Use the specialty filter in the sidebar to narrow results.

2 devices
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All2 General & Plastic Surgery 2