Biomedex, Inc.
Country not established
- Devices
- 1
What Biomedex, Inc. makes
Biomedex, Inc. manufactures skin test systems, including the DERMAPIK II system, individual DERMAPIK II single test devices, POLYPIK II multiple skin test devices, and DERMAPIK trays.
The company is based in the United States, and its portfolio of Class II medical devices is listed in the FDA 510(k) regulatory registry.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biomedex, Inc. have in the registry?
The registry currently lists 1 device for Biomedex, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biomedex, Inc.'s devices?
Among its 1 most recently registered device, Biomedex, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Biomedex, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Biomedex, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Biomedex, Inc. in the registry?
The most recently registered devices listed for Biomedex, Inc. include DERMAPIK II SKIN TEST SYSTEM, DERMAPIK II (SINGLE TEST DEVICE), POLYPIK II (MULTIPLE SKIN TEST DEVICE), DERMAPIK TRAY, D.