Poseidon Medical, Inc.
Country not established
- Devices
- 1
What Poseidon Medical, Inc. makes
Poseidon Medical, Inc. manufactures the Tryton Side Branch Stent, a vascular device designed for coronary artery interventions, specifically to address complex bifurcation lesions by providing support to side branches during stent placement.
The company’s products are regulated under Class III in the United States and are listed in the FDA’s Premarket Approval (PMA) registry. The manufacturer is based in the US.
Catalogue
Tryton Side Branch Stent Ref P150039
Regimes: PMA Registry: PMA
Frequently asked questions
How many devices does Poseidon Medical, Inc. have in the registry?
The registry currently lists 1 device for Poseidon Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Poseidon Medical, Inc.'s devices?
Among its 1 most recently registered device, Poseidon Medical, Inc. has devices listed in FDA PMA (1 device).
What risk classes do Poseidon Medical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Poseidon Medical, Inc.'s devices are Class III. Each device page shows its own class and authorisation.
What are the newest devices from Poseidon Medical, Inc. in the registry?
The most recently registered devices listed for Poseidon Medical, Inc. include Tryton Side Branch Stent.