Phantomics, Inc.
South KoreaFDA applicant, unverified
- Devices
- 2
What Phantomics, Inc. makes
Phantomics, Inc. manufactures diagnostic devices under the Myomics brand, including the Myomics and Myomics Q systems. These devices are designed for muscle tissue analysis, providing quantitative assessments of muscle health and function through specialized imaging and analysis techniques.
The company’s products fall under FDA Class II regulatory classification and are listed via the 510(k) clearance pathway in the United States. No additional registries or international authorizations are referenced in the available data.
Catalogue
Frequently asked questions
How many devices does Phantomics, Inc. have in the registry?
The registry currently lists 2 devices for Phantomics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Phantomics, Inc.'s devices?
Among its 2 most recently registered devices, Phantomics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Phantomics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Phantomics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Phantomics, Inc. in the registry?
The most recently registered devices listed for Phantomics, Inc. include Myomics and Myomics Q.