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Elos Medtech Pinol A/S

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
12
Inspections
3
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K251497Elos Accurate Hybrid BaseOctober 16, 2025
K242025Elos Accurate® Hybrid Base™December 10, 2024
K241722Elos Accurate® Hybrid Base™; Elos Accurate® Customized AbutmentSeptember 13, 2024
K231307Elos Accurate Customized AbutmentDecember 21, 2023
K230317Elos Accurate Hybrid BaseSeptember 1, 2023
K222044Elos Accurate Customized AbutmentNovember 30, 2022
K201860Elos Accurate Hybrid BaseFebruary 19, 2021
K191919Elos Accurate Hybrid BaseFebruary 10, 2020
K191890Elos Accurate Customized AbutmentFebruary 6, 2020
K192457Elos Accurate Customized AbutmentJanuary 2, 2020
K190299Elos Accurate® Customized AbutmentJune 26, 2019
K171799Elos Accurate Customized Abutment, Elos Prosthetic ScrewJanuary 15, 2018