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BIOSERENITY MEDICAL DEVICES GROUP

FDA registration: France Last updated 30 May 2026 Part of Bioserenity Medical Devices Group

Devices
33
Registries
GUDIDFDA
FDA recalls
0

Catalogue33

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Bioserenity Medical Devices Group PARIS CEDEX 13 Ile-de-France · FR FEI 3014027738

Frequently asked questions

How many devices does BIOSERENITY MEDICAL DEVICES GROUP have in the registry?

The registry currently lists 33 devices for BIOSERENITY MEDICAL DEVICES GROUP. Devices recorded under merged duplicate company entries are counted once.

Which registries list BIOSERENITY MEDICAL DEVICES GROUP's devices?

Among its 33 most recently registered devices, BIOSERENITY MEDICAL DEVICES GROUP has devices listed in FDA GUDID (33 devices).

What risk classes do BIOSERENITY MEDICAL DEVICES GROUP's devices fall under?

Among its 33 most recently registered devices, the classes recorded for BIOSERENITY MEDICAL DEVICES GROUP's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from BIOSERENITY MEDICAL DEVICES GROUP in the registry?

The most recently registered devices listed for BIOSERENITY MEDICAL DEVICES GROUP include Neuronaute 1.2 - BioAdapter 1001-15015-US, Neuronaute 1.2 - Battery charger 1001-15017-US, Neuronaute IceCap 1001-01010-US and Accusom 1017-15014-US.

Which FDA establishments are linked to BIOSERENITY MEDICAL DEVICES GROUP?

1 FDA establishment is linked to BIOSERENITY MEDICAL DEVICES GROUP in the registry; they are listed on the company page.

Generated automatically from registry data and not verified by a human reviewer.

Information

FDA registration
France(from the FDA establishment record (FEI))
DUNS number
281224773