Hans Hermann GmbH
GermanyFDA applicant, unverified
- Devices
- 2
What Hans Hermann GmbH makes
Hans Hermann GmbH manufactures titanium plating systems—including the Titanium Miniplating, Microplating, and Mediumplating systems (e.g., model H12-1010)—for orthopedic applications, as well as laparoscopic instruments and related accessories.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Hans Hermann Laparoscopes And Accessories Ref K051610
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hans Hermann GmbH have in the registry?
The registry currently lists 2 devices for Hans Hermann GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hans Hermann GmbH's devices?
Among its 2 most recently registered devices, Hans Hermann GmbH has devices listed in FDA 510(k) (2 devices).
What risk classes do Hans Hermann GmbH's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Hans Hermann GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hans Hermann GmbH in the registry?
The most recently registered devices listed for Hans Hermann GmbH include THE TITANIUM MINIPLATING SYSTEM, THE TITANIUM MICROPLATING SYSTEM, THE TITANIUM MEDIUMPLATING SYSTEM, MODEL #'S H12-1010 and HANS HERMANN LAPAROSCOPES AND ACCESSORIES.