Pierenkemper GmbH
GermanyFDA applicant, unverified
- Devices
- 1
What Pierenkemper GmbH makes
Pierenkemper GmbH manufactures the StimaWELL 120MTRS, a medical device designed for spinal stimulation or neuromodulation applications, likely intended for therapeutic use in pain management or neurological conditions.
The StimaWELL 120MTRS is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
StimaWELL 120MTRS Ref K181645
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pierenkemper GmbH have in the registry?
The registry currently lists 1 device for Pierenkemper GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pierenkemper GmbH's devices?
Among its 1 most recently registered device, Pierenkemper GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Pierenkemper GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Pierenkemper GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pierenkemper GmbH in the registry?
The most recently registered devices listed for Pierenkemper GmbH include StimaWELL 120MTRS.