Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Auris Surgical Robotics, Inc.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories1
Latest Approval2018-03-22
TypeNumberDevice NameCodeDate
510(k) K173760 Monarch Endoscopy Platform (Monarch Platform) EOQ 2018-03-22 View
510(k) K152319 Auris Robotic Endoscopy System (ARES) EOQ 2016-05-26 View