Orofacial Dynamics
Country not established
- Devices
- 1
What Orofacial Dynamics makes
Orofacial Dynamics manufactures the ORO-Facial Myographic Measurement Instrument (OMMI), a device designed for assessing and quantifying myographic activity in orofacial muscles. This instrument is used primarily for clinical and research applications to evaluate muscle function, potentially aiding in the diagnosis and treatment of conditions affecting facial and jaw muscles.
The OMMI is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) database. The company is headquartered in the United States, where its device portfolio is subject to U.S. regulatory oversight.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Orofacial Dynamics have in the registry?
The registry currently lists 1 device for Orofacial Dynamics. Devices recorded under merged duplicate company entries are counted once.
Which registries list Orofacial Dynamics's devices?
Among its 1 most recently registered device, Orofacial Dynamics has devices listed in FDA 510(k) (1 device).
What risk classes do Orofacial Dynamics's devices fall under?
Among its 1 most recently registered device, the classes recorded for Orofacial Dynamics's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Orofacial Dynamics in the registry?
The most recently registered devices listed for Orofacial Dynamics include ORO-FACIAL MYOGRAPHIC MEASUREMENT INSTRUMENT (OMMI).