Medical Device Manufacturer · US , Sarasota , FL

Medone Surgical, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2021
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
1-1 of 1
Filters
All1 Ophthalmic 1