Auris Surgical Robotics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Auris Surgical Robotics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Monarch Endoscopy Platform (Monarch Platform)
2
Total
2
Cleared
0
Denied
Auris Surgical Robotics, Inc. has 2 FDA 510(k) cleared medical devices. Based in San Carlos, US.
Historical record: 2 cleared submissions from 2016 to 2018. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Auris Surgical Robotics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Auris Surgical Robotics, Inc.
2 devices