Medone Surgical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medone Surgical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MicroDose Injector
1
Total
1
Cleared
0
Denied
Medone Surgical, Inc. has 1 FDA 510(k) cleared medical devices. Based in Sarasota, US.
Last cleared in 2021. Active since 2021. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Medone Surgical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Elkin Rc, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Medone Surgical, Inc.
1 devices