510(k) K231388

NextDent Base by Vertex-Dental B.V. — Product Code EBI

K231388 is an FDA 510(k) premarket notification submitted by Vertex-Dental B.V. for the device "NextDent Base". The FDA issued a decision of Substantially Equivalent on Oct 20, 2023. The device falls under product code EBI (Resin, Denture, Relining, Repairing, Rebasing), a Class II device regulated under 21 CFR 872.3760. Vertex-Dental B.V. has at least 7 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
Oct 20, 2023
Date Received
May 12, 2023
Clearance Type
Abbreviated
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Resin, Denture, Relining, Repairing, Rebasing
Device Class
Class II
Regulation Number
872.3760
Review Panel
DE
Submission Type