Allomedic
Country not established
- Devices
- 1
What Allomedic makes
Allomedic manufactures the RIESS-LUHR, a medical device designed for the treatment of chronic wounds, including diabetic foot ulcers and venous leg ulcers, through the application of negative pressure wound therapy.
The RIESS-LUHR is classified as a Class I device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Riess-Luhr Ref K811113
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Allomedic have in the registry?
The registry currently lists 1 device for Allomedic. Devices recorded under merged duplicate company entries are counted once.
Which registries list Allomedic's devices?
Among its 1 most recently registered device, Allomedic has devices listed in FDA 510(k) (1 device).
What risk classes do Allomedic's devices fall under?
Among its 1 most recently registered device, the classes recorded for Allomedic's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Allomedic in the registry?
The most recently registered devices listed for Allomedic include RIESS-LUHR.