Contralco
Country not established
- Devices
- 1
What Contralco makes
Contralco manufactures medical devices classified under Class I, including products such as the CONTRALCO device. These items are designed for general medical use without requiring substantial risk mitigation, such as basic surgical instruments or low-risk accessories.
The company’s portfolio is regulated under the FDA’s 510(k) clearance process, ensuring compliance with U.S. medical device standards. These devices are listed in the FDA’s 510(k) registry, and the manufacturer operates from the United States.
Catalogue
Contralco Ref K100879
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Contralco have in the registry?
The registry currently lists 1 device for Contralco. Devices recorded under merged duplicate company entries are counted once.
Which registries list Contralco's devices?
Among its 1 most recently registered device, Contralco has devices listed in FDA 510(k) (1 device).
What risk classes do Contralco's devices fall under?
Among its 1 most recently registered device, the classes recorded for Contralco's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Contralco in the registry?
The most recently registered devices listed for Contralco include CONTRALCO.