Oculus Optikgeräte GmbH

Oculus Optikgeräte GmbH holds 2 FDA 510(k) medical device clearances, first cleared 2021, most recent 2026.

Top product codes for Oculus Optikgeräte GmbH

MXK — Ophthalmic2 devices

Recent clearances by Oculus Optikgeräte GmbH

K251848 — Pentacam® Cornea OCTCode MXK·2026-03-13
K202989 — Myopia MasterCode MXK·2021-07-14

Data sourced from openFDA. This site is unofficial and independent of the FDA.