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Auris Robotic Endoscopy System (ARES)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K152319
510(k) Type
Traditional
Applicant
Auris Surgical Robotics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/2016
Days to Decision
283 days
Submission Type
Summary

Auris Robotic Endoscopy System (ARES)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K152319
510(k) Type
Traditional
Applicant
Auris Surgical Robotics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/2016
Days to Decision
283 days
Submission Type
Summary