Pleural Dynamics, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3029300753
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
What Pleural Dynamics, Inc. makes
Pleural Dynamics, Inc. makes the Automatic Continuous Effusion Shunt (ACES) System, a device designed for managing pleural effusions.
The ACES System is a Class II medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3029300753
- Address
- 601 Carlson Pkwy Ste 890, Minnetonka, MN, 55305
Frequently asked questions
How many devices does Pleural Dynamics, Inc. have in the registry?
The registry currently lists 3 devices for Pleural Dynamics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pleural Dynamics, Inc.'s devices?
Among its 3 most recently registered devices, Pleural Dynamics, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Pleural Dynamics, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Pleural Dynamics, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pleural Dynamics, Inc. in the registry?
The most recently registered devices listed for Pleural Dynamics, Inc. include Automatic Continuous Effusion Shunt (ACES) System AS16-7, Automatic Continuous Effusion System (ACES) Kit AK01-1 and Automatic Continuous Effusion Shunt (ACES) System ACES System.