Mariner Endosurgery, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Mariner Endosurgery, Inc. - FDA 510(k) Cleared Devices
Recent clearances: LaparoGuard
1
Total
1
Cleared
0
Denied
Mariner Endosurgery, Inc. has 1 FDA 510(k) cleared medical devices. Based in Hamilton, CA.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Mariner Endosurgery, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Ironstone Product Development, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Mariner Endosurgery, Inc.
1 devices