Dewin

Dewin Fertilization Medium is intended for use during vitro fertilization (IVF) procedures and culture to the two pronuclei (zygote) stage of development. Dewin Fertilization Medium is also…

Registry build 21.09.26

Dewin Fertilization Medium is intended for use during vitro fertilization (IVF) procedures and culture to the two pronuclei (zygote) stage of development. Dewin Fertilization Medium is also intended for washing and handling sperm and collected oocytes after aspiration prior to IVF procedures. Dewin Fertilization Medium is not intended for use in intrauterine insemination procedures.

4manufacturers in China registered for this device type
8catalogue numbers in this listing
4510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (3), Shandong (1).

Chinese manufacturers registered for FDA product code MQL
Manufacturer City Province Registered as Device types
Dongguan King Medical Technology Co., Ltd. Dongguan Guangdong Contract manufacturer 14
Shenzhen VitaVitro Biotech Co., Ltd. Shenzhen Guangdong Manufacturer 7
Gimbo Medical Technology Shenzhen Co., Ltd. Shenzhen Guangdong Manufacturer 3
Shandong Wego Ruisheng Medical Device Co., Ltd. Weihai Shandong Manufacturer 2

Record

Regulatory record for Dewin
Listed by Donnevie Medical Technology (Shanghai) Co., Ltd., China
FDA product code MQL
Device type Media, Reproductive
Device class Class 2
Regulation 21 CFR 884.6180
Establishment Manufacturer
510(k) K212426
Record published 2022-07-08

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date

Catalogue Numbers

Catalogue numbers for Dewin
Catalogue number Size Status
9342 In distribution
9311 In distribution
9310 In distribution
9326 In distribution
9341 In distribution
9327 In distribution
9343 In distribution
9340 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
LifeGlobal® Media LifeGlobal Group, LLC 93
Sydney IVF William A. Cook Australia PTY, Ltd. 29
LifeGlobal® Media Coopersurgical, Inc. 27
VitaVitro Shenzhen VitaVitro Biotech Co., Ltd. 22
Nidacon Nidacon International AB 19
Sil-Select Plus Lower Layer Fertipro NV 8
FertiCult Mineral Oil Fertipro NV 8
SpermGrad Vitrolife Sweden AB 8
Sequential Culture Media Kitazato Corporation 8
Sperm Wash Medium Invitrocare Inc 7
Enhance-S Plus Vitrolife Inc. 7
G-Vitri™ Vitrification media Gimbo Medical Technology Shenzhen Co., Ltd. 7

Showing 12 of 360. All products under Media, Reproductive

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K251637 2025-08-27
K242561 2025-04-10
K231370 2023-08-04
K212426 2022-06-16

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer