Leibinger & Fischer, Ltd.
Country not established
- Devices
- 3
What Leibinger & Fischer, Ltd. makes
Leibinger & Fischer, Ltd. manufactures the NEURO N 50 LESION GENERATOR, a device used for controlled tissue ablation in neurosurgical procedures, and the STP COMPLETE MODULE SET, a system for spinal fixation and stabilization.
These products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Micro Multileaf Collimator Ref K943714
Regimes: 510(k) Registry: 510(k)Neuro N 50 Lesion Generator Ref K896450
Regimes: 510(k) Registry: 510(k)Stp Complete Module Set Ref K892425
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Leibinger & Fischer, Ltd. have in the registry?
The registry currently lists 3 devices for Leibinger & Fischer, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Leibinger & Fischer, Ltd.'s devices?
Among its 3 most recently registered devices, Leibinger & Fischer, Ltd. has devices listed in FDA 510(k) (3 devices).
What risk classes do Leibinger & Fischer, Ltd.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Leibinger & Fischer, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Leibinger & Fischer, Ltd. in the registry?
The most recently registered devices listed for Leibinger & Fischer, Ltd. include MICRO MULTILEAF COLLIMATOR, NEURO N 50 LESION GENERATOR and STP COMPLETE MODULE SET.