Shenzhen Vitavitro Biotech Co., Ltd.
Shenzhen Vitavitro Biotech Co., Ltd. has 0 FDA recalls, 0 inspections, 5 510(k) clearances and 0 compliance actions on record.
- Latest 510(k)
- Nov 15, 2024
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Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Oct 23, 2026 | Not stated | Current |
| 510(k) clearances | 5 | Oct 4, 2026 | Not stated | Current |
| Inspections | 0 | Oct 25, 2026 | Not stated | Current |
| Compliance actions | 0 | Oct 23, 2026 | Not stated | Current |
Related names
| Name | Recalls | 510(k) | Inspections | Compliance | Most recent recall |
|---|---|---|---|---|---|
| Shenzhen Vitavitro Bio-Tech Co | 0 | 1 | 0 | 0 | — |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K240523 | VitaVitro® Single Lumen Oocyte Retrieval Needle (ORNS-17G, ORNS-18G), VitaVitro® Double Lumen Oocyte… | Nov 15, 2024 |
| K240307 | VitaVitro Embryo Transfer Catheter (Models ET-S, ET-SI, ET-A, ET-I, ET-IH) | Aug 16, 2024 |
| K212410 | VitaVitro Sperm Washing Medium, VitaVitro Sperm Gradient Medium | Feb 1, 2022 |
| K200408 | VitaVitro® Fertilization Medium, VitaVitro® Gamete Buffer Medium, VitaVitro® Flushing Buffer Medium | Oct 16, 2020 |
| K191063 | 1-Step Culture Medium | Aug 23, 2019 |