Plexus Biomedical, Inc.
Country not established
- Devices
- 1
What Plexus Biomedical, Inc. makes
Plexus Biomedical, Inc. manufactures the HEM-AVERT perianal stabilizer.
This device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Hem-Avert Perianal Stabilizer Ref DEN090011
Regimes: De Novo Registry: De Novo
Frequently asked questions
How many devices does Plexus Biomedical, Inc. have in the registry?
The registry currently lists 1 device for Plexus Biomedical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Plexus Biomedical, Inc.'s devices?
Among its 1 most recently registered device, Plexus Biomedical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Plexus Biomedical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Plexus Biomedical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Plexus Biomedical, Inc. in the registry?
The most recently registered devices listed for Plexus Biomedical, Inc. include HEM-AVERT PERIANAL STABILIZER.