Medical Device Manufacturer · CN , Shenzhen

Shenzhen Vitavitro Biotech Co., Ltd. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2019
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
1–5 of 5
VitaVitro? Single Lumen Oocyte Retrieval Needle (ORNS-17G, ORNS-18G), VitaVitro? Double Lumen Oocyte Retrieval Needle (ORND-17G)
K240523 · MQE Needle, Assisted Reproduction · Obstetrics & Gynecology
Nov 2024 266d
VitaVitro Embryo Transfer Catheter (Models ET-S, ET-SI, ET-A, ET-I, ET-IH)
K240307 · MQF Catheter, Assisted Reproduction · Obstetrics & Gynecology
Aug 2024 196d
VitaVitro Sperm Washing Medium, VitaVitro Sperm Gradient Medium
K212410 · MQL Media, Reproductive · Obstetrics & Gynecology
Feb 2022 182d
VitaVitro? Fertilization Medium, VitaVitro? Gamete Buffer Medium, VitaVitro? Flushing Buffer Medium
K200408 · MQL Media, Reproductive · Obstetrics & Gynecology
Oct 2020 240d
1-Step Culture Medium
K191063 · MQL Media, Reproductive · Obstetrics & Gynecology
Aug 2019 123d
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