Markoptic
Country not established
- Devices
- 2
What Markoptic makes
Markoptic designs and manufactures arthroscopes, including models described as improved arthroscopes. These devices are used in minimally invasive orthopedic procedures to visualize and operate within joints, such as the knee or shoulder.
The company’s arthroscopes fall under Class II regulatory classification in the US, requiring 510(k) clearance through the FDA. These devices are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Markoptic Improved Arthroscope Ref K860607
Regimes: 510(k) Registry: 510(k)Improved Arthroscope Ref K830120
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Markoptic have in the registry?
The registry currently lists 2 devices for Markoptic. Devices recorded under merged duplicate company entries are counted once.
Which registries list Markoptic's devices?
Among its 2 most recently registered devices, Markoptic has devices listed in FDA 510(k) (2 devices).
What risk classes do Markoptic's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Markoptic's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Markoptic in the registry?
The most recently registered devices listed for Markoptic include MARKOPTIC IMPROVED ARTHROSCOPE and IMPROVED ARTHROSCOPE.