# Auris Surgical Robotics, Inc.

- Location (FDA's records): San Carlos, CA
- FDA decisions: 2 (2016–2018): 2 510(k) clearances
- Product codes: EOQ (2)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- KARL STORZ Endoscopy-America, Inc.: 2 (https://510kreport.com/company/karl-storz-endoscopy-america)
- Spiration, Inc.: 1 (https://510kreport.com/company/spiration)
- Olympus America, Inc.: 1 (https://510kreport.com/company/olympus-america)
- Mill-Rose Laboratory: 1 (https://510kreport.com/company/mill-rose-laboratory)

## Firms that cite its devices most
- Noah Medical Corp.: 1 (https://510kreport.com/company/noah-medical)
- Auris Health, Inc.: 1 (https://510kreport.com/company/auris-health)

## Its most-cited devices
- K173760: Monarch Endoscopy Platform (Monarch Platform) (2018), cited by 2

## Recent decisions
- K173760: Monarch Endoscopy Platform (Monarch Platform) (Mar 22, 2018)
- K152319: Auris Robotic Endoscopy System (ARES) (May 26, 2016)

Source page: https://510kreport.com/company/auris-surgical-robotics