Pharmascience, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Pharmascience, Inc. makes
Pharmascience, Inc. manufactures DURAFLOR, a medical device designed for use in surgical procedures, specifically as a vascular graft or similar implant material.
The company’s portfolio is regulated under Class II devices in the US, with DURAFLOR authorised via the FDA’s 510(k) pathway. The devices are listed in the FDA’s 510(k) registry.
Catalogue
Frequently asked questions
How many devices does Pharmascience, Inc. have in the registry?
The registry currently lists 2 devices for Pharmascience, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pharmascience, Inc.'s devices?
Among its 2 most recently registered devices, Pharmascience, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Pharmascience, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Pharmascience, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pharmascience, Inc. in the registry?
The most recently registered devices listed for Pharmascience, Inc. include DURAFLOR.