Oculus Optikgeraete GMBH
4 recalls on record · Latest: Sep 6, 2023
FDA Devices Moderate Sep 6, 2023
Oculus Pentacam AXL , Ref 70100, CE 0123
FDA Devices Moderate Sep 6, 2023
Oculus Myopia Master , Ref 68100, CE 0123
FDA Devices Moderate Sep 7, 2022
Pentacam AXL REF 70100, Pentacam HR REF 70900. Used to image the anterior segment of the eye.
FDA Devices Moderate Feb 28, 2018