Medical Device Manufacturer · FR , Paris

Bioserenity - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2017

2

Total

2

Cleared

0

Denied

Bioserenity has 2 FDA 510(k) cleared medical devices. Based in Paris, FR.

Last cleared in 2023. Active since 2017. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Bioserenity Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Bioserenity

2 devices

1-2 of 2

Cleared Jan 12, 2023

Neuronaute with IceCap 2 & IceCap 2 Small

Neurology · 37d

Cleared Dec 26, 2017

Neurology · 343d