Shenzhen Vitavitro Biotech Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: VitaVitro® Single Lumen Oocyte Retrieval Needle (ORNS-17G, ORNS-18G), VitaVitro® Double Lumen Oocyte Retrieval Needle (ORND-17G), VitaVitro Embryo Transfer Catheter (Models ET-S, ET-SI, ET-A, ET-I, ET-IH), VitaVitro Sperm Washing Medium, VitaVitro Sperm Gradient Medium
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Shenzhen Vitavitro Biotech Co., Ltd. Obstetrics & Gynecology ✕
5 devices
Cleared
Nov 15, 2024
VitaVitro® Single Lumen Oocyte Retrieval Needle (ORNS-17G, ORNS-18G),...
Obstetrics & Gynecology
266d
Cleared
Aug 16, 2024
VitaVitro Embryo Transfer Catheter (Models ET-S, ET-SI, ET-A, ET-I, ET-IH)
Obstetrics & Gynecology
196d
Cleared
Feb 01, 2022
VitaVitro Sperm Washing Medium, VitaVitro Sperm Gradient Medium
Obstetrics & Gynecology
182d
Cleared
Oct 16, 2020
VitaVitro® Fertilization Medium, VitaVitro® Gamete Buffer Medium, VitaVitro®...
Obstetrics & Gynecology
240d
Cleared
Aug 23, 2019
1-Step Culture Medium
Obstetrics & Gynecology
123d