Quantalx Neuroscience
IsraelFDA applicant, unverified FDA FEI 3020494684
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Quantalx Neuroscience makes
Quantalx Neuroscience manufactures the Delphi Stimulator, which is a Class II medical device.
The company is based in the US and the Delphi Stimulator is listed in the FDA 510(k) registry.
Catalogue
Delphi-MD System Ref DEN250002
Regimes: De Novo Registry: De NovoDelphi MCS Electrode Cap Ref K243243
Regimes: 510(k) Registry: 510(k)Delphi Stimulator Ref K242345
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3020494684
- Address
- 1 Hatachana st., Kfar Saba Central
Frequently asked questions
How many devices does Quantalx Neuroscience have in the registry?
The registry currently lists 3 devices for Quantalx Neuroscience. Devices recorded under merged duplicate company entries are counted once.
Which registries list Quantalx Neuroscience's devices?
Among its 3 most recently registered devices, Quantalx Neuroscience has devices listed in FDA 510(k) (3 devices).
What risk classes do Quantalx Neuroscience's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Quantalx Neuroscience's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Quantalx Neuroscience in the registry?
The most recently registered devices listed for Quantalx Neuroscience include Delphi-MD System, Delphi MCS Electrode Cap and Delphi Stimulator.