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Vitromed GmbH

FDA Regulatory Profile

Summary

Total Recalls: 0
510(k) Clearances: 7
Inspections: 1
Compliance Actions: 0

Recent 510(k) Clearances

K-Number	Device	Date
K241833	V-GRAD	March 21, 2025
K240176	V-VITFREEZE and V-VITWARM	September 13, 2024
K232125	V-PVP	March 20, 2024
K222606	V-HYADASE	May 26, 2023
K223117	V-SPERM WASH	January 31, 2023
K193285	V-ONESTEP	November 20, 2020
K192146	V-DENUPET	January 28, 2020