Medical Device Manufacturer · DK , Goerloese

Elos Medtech Pinol A/S - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 2018

Recent clearances: Elos Accurate Hybrid Base, Elos Accurate® Denture Fixation System, Elos Accurate Hybrid Base

14
Total
14
Cleared
0
Denied

Elos Medtech Pinol A/S has 14 FDA 510(k) cleared dental devices. Based in Goerloese, DK.

Latest FDA clearance: Sep 2026. Active since 2018.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by PaxMed International, LLC as regulatory consultant.

FDA 510(k) Regulatory Record - Elos Medtech Pinol A/S

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