Oculus Optikgeräte GmbH

FDA Regulatory Profile

Oculus Optikgeräte GmbH appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 13, 2026.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K251848Pentacam® Cornea OCTMarch 13, 2026
K202989Myopia MasterJuly 14, 2021