Biotech companyLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in ChinaLabelled 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 15, 2026, FDA's public records list Shenzhen Vitavitro Biotech with 5 510(k) clearances. The most recent is a 510(k) clearance dated Nov 15, 2024: VitaVitro® Single Lumen Oocyte Retrieval Needle (ORNS-17G, ORNS-18G), VitaVitro® Double ….
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.
| Nov 15, 2024 | VitaVitro® Single Lumen Oocyte Retrieval Needle (ORNS-17G, ORNS-18G), VitaVitro® Double Lumen Oocyte Retrieval Needle (ORND-17G)K240523 · MQE | 510(k) clearances |
| Aug 16, 2024 | VitaVitro Embryo Transfer Catheter (Models ET-S, ET-SI, ET-A, ET-I, ET-IH)K240307 · MQF | 510(k) clearances |
| Feb 1, 2022 | VitaVitro Sperm Washing Medium, VitaVitro Sperm Gradient MediumK212410 · MQL | 510(k) clearances |
| Oct 16, 2020 | VitaVitro® Fertilization Medium, VitaVitro® Gamete Buffer Medium, VitaVitro® Flushing Buffer MediumK200408 · MQL | 510(k) clearances |
| Aug 23, 2019 | 1-Step Culture MediumK191063 · MQL | 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
