Lorenz Biotech S.p.A.
Country not established
- Devices
- 2
What Lorenz Biotech S.p.A. makes
Lorenz Biotech S.P.A. manufactures single-use foam and non-woven adhesive electrodes for electrotherapy applications, including models 800-000-057 and 800-000-058. The company also produces the APTIVA software system, version 2.13, designed for electrotherapy device control and monitoring.
These products fall under Class II medical device classification in the US and are listed via 510(k) clearance with the FDA. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Lorenz Biotech Aptiva, Version 2.13 Ref K061828
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lorenz Biotech S.P.A. have in the registry?
The registry currently lists 2 devices for Lorenz Biotech S.P.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lorenz Biotech S.P.A.'s devices?
Among its 2 most recently registered devices, Lorenz Biotech S.P.A. has devices listed in FDA 510(k) (2 devices).
What risk classes do Lorenz Biotech S.P.A.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Lorenz Biotech S.P.A.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lorenz Biotech S.P.A. in the registry?
The most recently registered devices listed for Lorenz Biotech S.P.A. include FREMS SSC DISPOSABLE FOAM ELECTRODES, MODEL 800-000-057; FREMS SSC DISPOSABLE NON-WOVEN ELECTRODES, MODEL 800-000-058 and LORENZ BIOTECH APTIVA, VERSION 2.13.