Clinical House Europe GmbH
Country not established
- Devices
- 2
What Clinical House Europe GmbH makes
Clinical House Europe GmbH manufactures dental diagnostic devices, including the PERIOTYPE X-PERT and PerioType Rapid, which are designed for periodontal disease assessment and monitoring. These tools provide imaging and analysis capabilities to evaluate bone loss and gum health in patients.
The company’s portfolio is regulated under Class II medical devices in the US, with products listed via the FDA’s 510(k) clearance process. The devices are intended for use in dental and oral health settings.
Catalogue
Periotype X-Pert Ref K123386
Regimes: 510(k) Registry: 510(k)PerioType Rapid Ref K143758
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Clinical House Europe GmbH have in the registry?
The registry currently lists 2 devices for Clinical House Europe GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Clinical House Europe GmbH's devices?
Among its 2 most recently registered devices, Clinical House Europe GmbH has devices listed in FDA 510(k) (2 devices).
What risk classes do Clinical House Europe GmbH's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Clinical House Europe GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Clinical House Europe GmbH in the registry?
The most recently registered devices listed for Clinical House Europe GmbH include PERIOTYPE X-PERT and PerioType Rapid.