Dr. Harold Bergman
CanadaFDA 510(k) applicant, unverified
- Devices
- 1
What Dr. Harold Bergman makes
Dr. Harold Bergman manufactures the EOH 8501 Osseointegrated Implant System, a device designed for osseointegration in orthopedic or dental applications.
The EOH 8501 Osseointegrated Implant System is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The manufacturer operates from the United States.
Catalogue
Eoh 8501 Osseointegrated Implant System Ref K861502
510(k) 510(k)
Frequently asked questions
How many devices does Dr. Harold Bergman have in the registry?
The registry currently lists 1 device for Dr. Harold Bergman. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dr. Harold Bergman's devices?
Among its 1 most recently registered device, Dr. Harold Bergman has devices listed in FDA 510(k) (1 device).
What risk classes do Dr. Harold Bergman's devices fall under?
Among its 1 most recently registered device, the classes recorded for Dr. Harold Bergman's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dr. Harold Bergman in the registry?
The most recently registered devices listed for Dr. Harold Bergman include EOH 8501 OSSEOINTEGRATED IMPLANT SYSTEM.