Nuxen S.R.L.
AR Last updated 22 Oct 2026
- Devices
- 2
- Registries
- FDA 510(k)
- FDA recalls
- 0
Catalogue
Deflex Acrilato Ref K113788
Deflex Ref K113608
What Nuxen S.R.L. makes
Nuxen S.R.L. manufactures DEFLEX ACRILATO and DEFLEX, which are Class II medical devices.
These devices are listed in the FDA 510(k) registry, and the company is based in the US.
Frequently asked questions
What medical devices does Nuxen S.R.L. manufacture?
Nuxen S.R.L. manufactures DEFLEX ACRILATO and DEFLEX, which are Class II medical devices. These devices are designed for specific medical applications as per their classification.
Where is Nuxen S.R.L. based?
Nuxen S.R.L. is based in the United States. The company operates from this location, manufacturing and distributing its medical devices to meet regulatory requirements.
Which regulatory registries list Nuxen S.R.L.'s devices?
Nuxen S.R.L.'s devices are listed in the FDA 510(k) registry. This indicates that they have been submitted for clearance through the FDA's premarket notification process.
How are Nuxen S.R.L.'s devices classified?
Nuxen S.R.L.'s devices, DEFLEX ACRILATO and DEFLEX, are classified as Class II medical devices. This classification indicates they require special controls to ensure their safety and effectiveness.
Information
- Country
- AR