Karl Leibinger GmbH U. Co. KG
Country not established
- Devices
- 1
What Karl Leibinger GmbH U. Co. KG makes
Karl Leibinger GmbH U. Co. KG manufactures the KLS-MARTIN Mandibular Fracture/Reconstruction System, a medical device designed for the fixation and stabilization of mandibular bone fractures and reconstructive procedures in oral and maxillofacial surgery.
The company’s portfolio is regulated under FDA 510(k) clearance as Class II devices. The system is listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Karl Leibinger GmbH U. Co. KG have in the registry?
The registry currently lists 1 device for Karl Leibinger GmbH U. Co. KG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Karl Leibinger GmbH U. Co. KG's devices?
Among its 1 most recently registered device, Karl Leibinger GmbH U. Co. KG has devices listed in FDA 510(k) (1 device).
What risk classes do Karl Leibinger GmbH U. Co. KG's devices fall under?
Among its 1 most recently registered device, the classes recorded for Karl Leibinger GmbH U. Co. KG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Karl Leibinger GmbH U. Co. KG in the registry?
The most recently registered devices listed for Karl Leibinger GmbH U. Co. KG include KLS-MARTIN MANDIBULAR FRACTURE/RECONSTRUCTION SYSTEM.