Symbion, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Symbion, Inc. makes
Symbion, Inc. manufactures medical devices, including a centrifugal blood pump and a sutureless temporary epicardial pacing lead.
The company's products are regulated as Class II devices and are listed in the FDA's 510(k) registry. Symbion is based in the United States.
Catalogue
Symbion Centrifugal Blood Pump Model I Ref K882129
Regimes: 510(k) Registry: 510(k)Sutureless Temporary Epicardial Pacing Lead Ref K873474
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Symbion, Inc. have in the registry?
The registry currently lists 2 devices for Symbion, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Symbion, Inc.'s devices?
Among its 2 most recently registered devices, Symbion, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Symbion, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Symbion, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Symbion, Inc. in the registry?
The most recently registered devices listed for Symbion, Inc. include SYMBION CENTRIFUGAL BLOOD PUMP MODEL I and SUTURELESS TEMPORARY EPICARDIAL PACING LEAD.