Symex Corp.
Country not established
- Devices
- 1
What Symex Corp. makes
Symex Corp. manufactures diagnostic reagents, including the VIRASTAT® FITC-labeled monoclonal antibody test for detecting parainfluenza viruses types 1, 2, and 3. These products are designed for laboratory use in identifying respiratory viral infections.
The company’s portfolio is regulated under Class I medical devices in the US, with relevant products listed via FDA 510(k) clearance. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Symex Corp. have in the registry?
The registry currently lists 1 device for Symex Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Symex Corp.'s devices?
Among its 1 most recently registered device, Symex Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Symex Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Symex Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Symex Corp. in the registry?
The most recently registered devices listed for Symex Corp. include VIRASTAT(R) FITC-LABEL ANTI-PARAINFLU 1, 2&3 MONO ANT.