Siegen Corp.
United StatesFDA applicant, unverified
- Devices
- 6
What Siegen Corp. makes
Siegen Corp. manufactures medical devices for neurological monitoring and stimulation, including the Siegen Visual Stimulator for visual evoked response testing, the Siegen Neuroscope and Neuroscope SEEG for intracranial electrophysiology, and disposable surface electrodes for EEG applications. Their product line also covers specialized headphones designed for neurophysiological assessments.
The company’s devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. These products are intended for use in clinical settings in the United States.
Catalogue
Siegen Visual Stimulator Ref K844616
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Siegen Surface Electrodes Ref K844646
Regimes: 510(k) Registry: 510(k)Siegen Neuroscope Ref K843464
Regimes: 510(k) Registry: 510(k)Siegen Headphones Ref K862430
Regimes: 510(k) Registry: 510(k)Neuroscope Seeg Ref K861884
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Siegen Corp. have in the registry?
The registry currently lists 6 devices for Siegen Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Siegen Corp.'s devices?
Among its 6 most recently registered devices, Siegen Corp. has devices listed in FDA 510(k) (6 devices).
What risk classes do Siegen Corp.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Siegen Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Siegen Corp. in the registry?
The most recently registered devices listed for Siegen Corp. include SIEGEN VISUAL STIMULATOR, SIEGEN NEUROSCOPE SEEG FOR EVOKED RESPONSE STIMU., SIEGEN SURFACE ELECTRODES and SIEGEN NEUROSCOPE.