Intermedics/Infusaid, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Intermedics/Infusaid, Inc. makes
Intermedics/Infusaid, Inc. manufactures implantable port systems and related explant kits, including the Infuse-A-Port (modified), Micro Port, and Infuse-A-Port Explant Kit.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Infuse-A-Port Explant Kit Ref K863296
Regimes: 510(k) Registry: 510(k)Infusaid Infuse-A-Port (Modified) Ref K853981
Regimes: 510(k) Registry: 510(k)Micro Port Ref K862018
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Intermedics/Infusaid, Inc. have in the registry?
The registry currently lists 3 devices for Intermedics/Infusaid, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Intermedics/Infusaid, Inc.'s devices?
Among its 3 most recently registered devices, Intermedics/Infusaid, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Intermedics/Infusaid, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Intermedics/Infusaid, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Intermedics/Infusaid, Inc. in the registry?
The most recently registered devices listed for Intermedics/Infusaid, Inc. include INFUSE-A-PORT EXPLANT KIT, INFUSAID INFUSE-A-PORT (MODIFIED) and MICRO PORT.