Excitus AS
NO Last updated 22 Oct 2026
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- Devices
- 1
- Registries
- FDA 510(k)
- FDA recalls
- 0
Catalogue
Cary Ref K251111
What Excitus AS makes
Excitus AS manufactures the Cary, a medical device designed for the treatment of chronic pain through spinal cord stimulation.
The Cary is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Frequently asked questions
What types of medical devices does Excitus AS manufacture?
Excitus AS specializes in the Cary, a device intended for chronic pain management. Specifically, it uses spinal cord stimulation to help alleviate symptoms in patients with certain types of persistent pain conditions.
Where is Excitus AS based?
Excitus AS is headquartered in the United States. The company’s location is relevant for understanding its regulatory framework and market focus.
How are Excitus AS’s devices classified under FDA regulations?
The Cary, Excitus AS’s primary device, is classified as a Class II medical device by the FDA. This classification typically indicates moderate risk, requiring special controls beyond general controls to ensure safety and effectiveness.
Which regulatory registries or databases list Excitus AS’s devices?
Excitus AS’s devices, including the Cary, are listed via the FDA’s 510(k) pathway. This pathway demonstrates that the device is substantially equivalent to a legally marketed predicate device, allowing it to enter the market.
Information
- Country
- NO