Lmv, Liske & Methling, GmbH
GermanyFDA applicant, unverified
- Devices
- 1
What Lmv, Liske & Methling, GmbH makes
Lmv, Liske & Methling, GmbH manufactures the FORMOSTAR, a medical device designed for precise imaging or diagnostic purposes in radiology.
The FORMOSTAR 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
Formostar Ref K862106
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lmv, Liske & Methling, GmbH have in the registry?
The registry currently lists 1 device for Lmv, Liske & Methling, GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lmv, Liske & Methling, GmbH's devices?
Among its 1 most recently registered device, Lmv, Liske & Methling, GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Lmv, Liske & Methling, GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Lmv, Liske & Methling, GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lmv, Liske & Methling, GmbH in the registry?
The most recently registered devices listed for Lmv, Liske & Methling, GmbH include FORMOSTAR.