Grumpy Innovation, Inc.
United Statesfrom the FDA registration address FDA FEI 3044675089
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Grumpy Innovation, Inc. makes
Grumpy Innovation, Inc. manufactures the Portare System, a medical device designed for [specific clinical purpose implied by the name, e.g., portable infusion or monitoring], intended for [brief use case, e.g., home or ambulatory patient care].
The Portare System is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Portare System (FA-001) Ref K243639
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3044675089
- Address
- 100 E 6th St, Sioux Falls, SD, 57104
Frequently asked questions
How many devices does Grumpy Innovation, Inc. have in the registry?
The registry currently lists 1 device for Grumpy Innovation, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Grumpy Innovation, Inc.'s devices?
Among its 1 most recently registered device, Grumpy Innovation, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Grumpy Innovation, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Grumpy Innovation, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Grumpy Innovation, Inc. in the registry?
The most recently registered devices listed for Grumpy Innovation, Inc. include Portare System (FA-001).