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.
FDA 510(k) cleared devices by Shenzhen Vitavitro Biotech Co., Ltd.
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