Shenzhen Vitavitro Biotech Co., Ltd. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Shenzhen Vitavitro Biotech Co., Ltd. has 5 FDA 510(k) cleared medical devices. Based in Shenzhen, CN.
Latest FDA clearance: Nov 2024. Active since 2019. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Shenzhen Vitavitro Biotech Co., Ltd. Filter by specialty or product code using the sidebar.
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