Vitromed GmbH
FDA Regulatory Profile
Vitromed GmbH appears in FDA public data with 0 recalls, 7 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 21, 2025.
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 |