Phraxis, Inc.
Country not established
- Devices
- 2
What Phraxis, Inc. makes
Phraxis, Inc. manufactures synthetic vascular grafts, including the EndoForce and its connector for endovascular venous anastomosis. These devices are designed for vascular reconstruction and anastomotic repair in surgical and interventional procedures.
The company’s products are classified as Class III medical devices under US regulations and are listed in the FDA’s Premarket Approval (PMA) and Unique Device Identifier (UDI) databases. The manufacturer operates from the United States.
Catalogue
- Registry: GUDID
- Regimes: PMA Registry: PMA
Company details
- DUNS number
- 825429017
- [email protected]
- Phone
- 8043574772
Frequently asked questions
How many devices does Phraxis, Inc. have in the registry?
The registry currently lists 2 devices for Phraxis, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Phraxis, Inc.'s devices?
Among its 2 most recently registered devices, Phraxis, Inc. has devices listed in FDA PMA (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Phraxis, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Phraxis, Inc.'s devices are Class III. Each device page shows its own class and authorisation.
What are the newest devices from Phraxis, Inc. in the registry?
The most recently registered devices listed for Phraxis, Inc. include EndoForce EFORCE-100 and EndoForce™ Connector for Endovascular Venous Anastomosis.