NextDent Denture, E-Denture
K-Number: K162572 · 2017-06-30
ApplicantVertex-Dental B.V.
Decision Date2017-06-30
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
NextDent Denture, E-Denture is a medical device manufactured by Vertex-Dental B.V.. It received FDA 510(k) clearance on 2017-06-30 under approval number K162572. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
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. It is manufactured by Vertex-Dental B.V.. The 510(k) number is K162572.
When was NextDent Denture, E-Denture approved by the FDA?
NextDent Denture, E-Denture received FDA 510(k) clearance on 2017-06-30, under approval number K162572.
What company makes NextDent Denture, E-Denture?
NextDent Denture, E-Denture is manufactured by Vertex-Dental B.V..
What is the FDA product code for NextDent Denture, E-Denture?
The FDA product code for NextDent Denture, E-Denture is EBI.
Other Devices by Vertex-Dental B.V.
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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.