Dr. Bernard Loewenthal
Country not established
- Devices
- 1
What Dr. Bernard Loewenthal makes
Dr. Bernard Loewenthal manufactures the PERIO-TEST, a diagnostic device used in periodontal assessments to evaluate gingival crevicular fluid flow, aiding in the detection of periodontal disease.
The PERIO-TEST is classified as a Class I medical device in the US and is listed under the FDA’s 510(k) pathway. The manufacturer operates from the United States.
Catalogue
Perio-Test Ref K872215
510(k) 510(k)
Frequently asked questions
How many devices does Dr. Bernard Loewenthal have in the registry?
The registry currently lists 1 device for Dr. Bernard Loewenthal. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dr. Bernard Loewenthal's devices?
Among its 1 most recently registered device, Dr. Bernard Loewenthal has devices listed in FDA 510(k) (1 device).
What risk classes do Dr. Bernard Loewenthal's devices fall under?
Among its 1 most recently registered device, the classes recorded for Dr. Bernard Loewenthal's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Dr. Bernard Loewenthal in the registry?
The most recently registered devices listed for Dr. Bernard Loewenthal include PERIO-TEST.