NextDent Denture, E-Denture
K-Number: K162572 · 2017-06-30
Device Summary
Frequently Asked Questions
What is the NextDent Denture, E-Denture?
NextDent Denture, E-Denture is a medical device that received FDA 510(k) clearance on 2017-06-30. The listed applicant is Vertex-Dental B.V.. The 510(k) number is K162572.
When did NextDent Denture, E-Denture receive FDA 510(k) clearance?
NextDent Denture, E-Denture received FDA 510(k) clearance on 2017-06-30, under 510(k) number K162572.
Who is the listed applicant for NextDent Denture, E-Denture?
The FDA 510(k) record lists Vertex-Dental B.V. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NextDent Denture, E-Denture?
The FDA product code for NextDent Denture, E-Denture is EBI.
Other records listing Vertex-Dental B.V. 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: EBI)
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.