Matrix Electromedical, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Matrix Electromedical, Inc. makes
Matrix Electromedical, Inc. manufactures electrosurgical devices, including the MATRIX PRO-ELECDT and the MATRIX ELECDT & VACUPULLS. These products are designed for electrosurgical procedures and include vacuum-assisted components for tissue management.
The company’s portfolio consists of Class II devices, all of which are listed under the FDA’s 510(k) pathway. These products are regulated under US medical device laws and are based in the United States.
Catalogue
Matrix Pro-Elecdt Ref K930263
Regimes: 510(k) Registry: 510(k)Matrix Elecdt & Vacupulls Ref K930264
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Matrix Electromedical, Inc. have in the registry?
The registry currently lists 2 devices for Matrix Electromedical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Matrix Electromedical, Inc.'s devices?
Among its 2 most recently registered devices, Matrix Electromedical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Matrix Electromedical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Matrix Electromedical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Matrix Electromedical, Inc. in the registry?
The most recently registered devices listed for Matrix Electromedical, Inc. include MATRIX PRO-ELECDT and MATRIX ELECDT & VACUPULLS.