FDA 510(k) Applications Submitted by Elos Medtech Pinol A/S

FDA 510(k) Number Submission Date Device Name Applicant
K230317 02/06/2023 Elos Accurate Hybrid Base Elos Medtech Pinol A/S
K222044 07/11/2022 Elos Accurate Customized Abutment Elos Medtech Pinol A/S
K190299 02/11/2019 Elos Accurate« Customized Abutment Elos Medtech Pinol A/S
K171799 06/16/2017 Elos Accurate Customized Abutment, Elos Prosthetic Screw Elos Medtech Pinol A/S
K201860 07/06/2020 Elos Accurate Hybrid Base Elos Medtech Pinol A/S
K191890 07/15/2019 Elos Accurate Customized Abutment Elos Medtech Pinol A/S
K191919 07/18/2019 Elos Accurate Hybrid Base Elos Medtech Pinol A/S
K192457 09/09/2019 Elos Accurate Customized Abutment Elos Medtech Pinol A/S


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