Medical Device Manufacturer · DK , Goerloese

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

13 submissions · 13 cleared · Since 2018

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

13
Total
13
Cleared
0
Denied

Elos Medtech Pinol A/S has 13 FDA 510(k) cleared dental devices. Based in Goerloese, DK.

Latest FDA clearance: May 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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