Epilog
BelgiumFDA applicant, unverified
- Devices
- 1
What Epilog makes
Epilog manufactures the PreOp system, a medical device designed for preoperative planning and simulation in surgical procedures, enabling detailed visualization and assessment of anatomical structures.
The PreOp system is classified as a Class II device under FDA regulations and is authorised via the 510(k) clearance process. The company is based in the United States.
Catalogue
PreOp Ref K172858
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Epilog have in the registry?
The registry currently lists 1 device for Epilog. Devices recorded under merged duplicate company entries are counted once.
Which registries list Epilog's devices?
Among its 1 most recently registered device, Epilog has devices listed in FDA 510(k) (1 device).
What risk classes do Epilog's devices fall under?
Among its 1 most recently registered device, the classes recorded for Epilog's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Epilog in the registry?
The most recently registered devices listed for Epilog include PreOp.