Ziterion
GermanyFDA 510(k) applicant, unverified
- Devices
- 1
What Ziterion makes
Ziterion manufactures the ZIT-Z, a medical device designed for targeted treatment of acne vulgaris through controlled delivery of benzoyl peroxide.
The ZIT-Z is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Zit-Z Ref K092507
510(k) 510(k)
Frequently asked questions
How many devices does Ziterion have in the registry?
The registry currently lists 1 device for Ziterion. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ziterion's devices?
Among its 1 most recently registered device, Ziterion has devices listed in FDA 510(k) (1 device).
What risk classes do Ziterion's devices fall under?
Among its 1 most recently registered device, the classes recorded for Ziterion's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ziterion in the registry?
The most recently registered devices listed for Ziterion include ZIT-Z.