Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in GermanyLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Vitromed with 7 510(k) clearances. The most recent is a 510(k) clearance dated Mar 21, 2025: V-GRAD.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Date | Record | Source |
|---|---|---|
| Mar 21, 2025 | V-GRADK241833 · MQL | 510(k) clearances |
| Sep 13, 2024 | V-VITFREEZE and V-VITWARMK240176 · MQL | 510(k) clearances |
| Mar 20, 2024 | V-PVPK232125 · MQL | 510(k) clearances |
| May 26, 2023 | V-HYADASEK222606 · MQL | 510(k) clearances |
| Jan 31, 2023 | V-SPERM WASHK223117 · MQL | 510(k) clearances |
| Nov 20, 2020 | V-ONESTEPK193285 · MQL | 510(k) clearances |
| Jan 28, 2020 | V-DENUPETK192146 · MQH | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
