UV Active Implant System
K-Number: K182194 · 2018-12-14
Device Summary
Frequently Asked Questions
What is the UV Active Implant System?
UV Active Implant System is a medical device that received FDA 510(k) clearance on 2018-12-14. The listed applicant is Dio Corporation. The 510(k) number is K182194.
When did UV Active Implant System receive FDA 510(k) clearance?
UV Active Implant System received FDA 510(k) clearance on 2018-12-14, under 510(k) number K182194.
Who is the listed applicant for UV Active Implant System?
The FDA 510(k) record lists Dio Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UV Active Implant System?
The FDA product code for UV Active Implant System is DZE.
Other records listing Dio Corporation as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: DZE)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.