ZyMot

Sperm Separation Device Natech 3mL 10 pack

Registry build 21.09.26
10manufacturers in China registered for this device type
10catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Guangdong (8), Hubei (1), Shandong (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code MQK
Manufacturer City Province Registered as Device types
Shenzhen Boomingshing Medical Device Co., Ltd. Shenzhen Guangdong Contract manufacturer 5
Shenzhen JPY ION-Tech. Co., Ltd. Shenzhen Guangdong Contract manufacturer 20
Dongguan King Medical Technology Co., Ltd. Dongguan Guangdong Contract manufacturer 14
Wuhan Huchuang Union Technology Co., Ltd. Wuhan Hubei Manufacturer 8
Shenzhen VitaVitro Biotech Co., Ltd. Shenzhen Guangdong Manufacturer 7
HUA YUE Medical Technology Co., Ltd. Guangzhou Guangdong Manufacturer 7
CGN Gray (Shenzhen) Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 5
Gimbo Medical Technology Shenzhen Co., Ltd. Shenzhen Guangdong Manufacturer 3
Guangzhou Hehong Biotech Co., Ltd. Guangzhou Guangdong Manufacturer 2
Shandong Wego Ruisheng Medical Device Co., Ltd. Weihai Shandong Manufacturer 2

Record

Regulatory record for ZyMot
Listed by DxNow Inc., United States
FDA product code MQK
Device type Labware, Assisted Reproduction
Device class Class 2
Regulation 21 CFR 884.6160
Establishment Repacker / relabeller
510(k) K173075
Record published 2021-02-25

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

Catalogue Numbers

Catalogue numbers for ZyMot
Catalogue number Size Per pack Status
Multi 850 microL 3 In distribution
Multi 3mL 3 In distribution
Multi 3mL 3 In distribution
Multi 3mL 10 In distribution
Multi 850 microL 3 In distribution
Multi 3mL 10 In distribution
ICSI 3 In distribution
Multi 850 microL 10 In distribution
Multi 850 microL 10 In distribution
ICSI 10 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Cryotec Reprolife Inc. 20
VitriGuard Origio A/S 16
G-Vitri™ Vitrification Straw Gimbo Medical Technology Shenzhen Co., Ltd. 15
LensHooke Sperm Separation Device Bonraybio Co., Ltd. 9
cryo-GO Vitrification Device Fujifilm Irvine Scientific 9
LifeGlobal® GPS® Dishware Coopersurgical, Inc. 7
LifeGlobal® GPS® Dishware LifeGlobal Group, LLC 7
Nest VT Cook Incorporated 5
Surestrip Allwin Medical Devices, Inc. 5
Minvitro Vitrification Straw Guangzhou Hehong Biotech Co., Ltd. 5
Rapid-i Kit Vitrolife Sweden AB 5
Surelock Allwin Medical Devices, Inc. 5

Showing 12 of 102. All products under Labware, Assisted Reproduction

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K173075 2018-03-08

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