H.A. Opotow Consulting
Country not established
- Devices
- 1
What H.A. Opotow Consulting makes
H.A. Opotow Consulting manufactures dental materials, specifically the ESPE KETAC-ENDO APLICAP, a device used for endodontic applications in dental procedures. This product is designed to facilitate the application of resin-based materials in root canal treatments, aiding in the sealing and restoration of treated teeth.
The ESPE KETAC-ENDO APLICAP is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company operates within the United States, adhering to domestic regulatory standards for dental devices.
Catalogue
Espe Ketac-Endo Aplicap Ref K911061
510(k) 510(k)
Frequently asked questions
How many devices does H.A. Opotow Consulting have in the registry?
The registry currently lists 1 device for H.A. Opotow Consulting. Devices recorded under merged duplicate company entries are counted once.
Which registries list H.A. Opotow Consulting's devices?
Among its 1 most recently registered device, H.A. Opotow Consulting has devices listed in FDA 510(k) (1 device).
What risk classes do H.A. Opotow Consulting's devices fall under?
Among its 1 most recently registered device, the classes recorded for H.A. Opotow Consulting's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from H.A. Opotow Consulting in the registry?
The most recently registered devices listed for H.A. Opotow Consulting include ESPE KETAC-ENDO APLICAP.