Incoba Ltd D/B/A Dynaris
Country not established
- Devices
- 1
What Incoba Ltd D/B/A Dynaris makes
Incoba Ltd (Dynaris) manufactures the Apogee, a medical device designed for use in surgical procedures, specifically as a powered surgical instrument for tissue manipulation or dissection.
The Apogee 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
Apogee Ref K200401
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Incoba Ltd D/B/A Dynaris have in the registry?
The registry currently lists 1 device for Incoba Ltd D/B/A Dynaris. Devices recorded under merged duplicate company entries are counted once.
Which registries list Incoba Ltd D/B/A Dynaris's devices?
Among its 1 most recently registered device, Incoba Ltd D/B/A Dynaris has devices listed in FDA 510(k) (1 device).
What risk classes do Incoba Ltd D/B/A Dynaris's devices fall under?
Among its 1 most recently registered device, the classes recorded for Incoba Ltd D/B/A Dynaris's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Incoba Ltd D/B/A Dynaris in the registry?
The most recently registered devices listed for Incoba Ltd D/B/A Dynaris include Apogee.