Naox Technologies SAS
FranceFDA applicant, unverified FDA FEI 3043014934
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Naox Technologies SAS makes
Naox Technologies Sas manufactures the NX01, a medical device designed for [specific application not detailed in data]. The product is intended for [clinical use or indication not specified in data].
The NX01 is classified as a Class II device under regulatory frameworks and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
NX01 (NX01) Ref K251550
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3043014934
- Address
- 62 rue mazarine, Paris Ile-de-France
Frequently asked questions
How many devices does Naox Technologies Sas have in the registry?
The registry currently lists 1 device for Naox Technologies Sas. Devices recorded under merged duplicate company entries are counted once.
Which registries list Naox Technologies Sas's devices?
Among its 1 most recently registered device, Naox Technologies Sas has devices listed in FDA 510(k) (1 device).
What risk classes do Naox Technologies Sas's devices fall under?
Among its 1 most recently registered device, the classes recorded for Naox Technologies Sas's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Naox Technologies Sas in the registry?
The most recently registered devices listed for Naox Technologies Sas include NX01 (NX01).