FDA 510(k), K162572, NextDent Denture, E-Denture
FDA 510(k), K162572, NextDent Denture, E-Denture
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510(K) Number: K162572
Device Name: NextDent Denture, E-Denture
Manufacturer: O. F. Beckeringh van Loenen
Device Classification Name: Resin, Denture, Relining, Repairing, Rebasing
Regulation Number: EBI
Classification Product Code: 09/15/2016
Date Received: 06/30/2017
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Dental
Device Name: NextDent Denture, E-Denture
Manufacturer: O. F. Beckeringh van Loenen
Device Classification Name: Resin, Denture, Relining, Repairing, Rebasing
Regulation Number: EBI
Classification Product Code: 09/15/2016
Date Received: 06/30/2017
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Dental
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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