IVC-TWO

IVC-TWO is a synthetic, defined culture medium intended for use in assisted reproductive technology procedures.The formulation of IVC-TWO is substantially equivalent to the glucose and…

Registry build 21.09.26

IVC-TWO is a synthetic, defined culture medium intended for use in assisted reproductive technology procedures.The formulation of IVC-TWO is substantially equivalent to the glucose and phosphate free HTF formulation published by Quinn et al (Quinn P, Moinipanah R, Steinberg J, Weathersbee P: Fertil Steril 1995;63:922-924). IVC-TWO is designed to support early stages of embryonic growth (up to four days post-fertilization). IVC-TWO has been formulated without phosphate, which may be detrimental to embryo blastocyst development. IVC-TWO may be used as a stand alone medium or as the first stage of a sequential medium protocol.

4manufacturers in China registered for this device type
1catalogue number
10510(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 IVC-TWO
Listed by Invitrocare Inc, United States
FDA product code MQL
Device type Media, Reproductive
Device class Class 2
Regulation 21 CFR 884.6180
Establishment Repacker / relabeller, Manufacturer
510(k) K000937
Record published 2016-09-24
Record revised 2018-07-06 (version 3)

Specifications

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

Catalogue Numbers

Catalogue numbers for IVC-TWO
Catalogue number Size Status
2008-V 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
Dewin Donnevie Medical Technology (Shanghai) Co., Ltd. 8
SpermGrad Vitrolife Sweden AB 8
Sequential Culture Media Kitazato Corporation 8
Sperm Wash Medium Invitrocare Inc 7
Enhance-S Plus Vitrolife Inc. 7

Showing 12 of 360. All products under Media, Reproductive

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K023222 2002-12-26
K003751 2001-01-17
K001967 2000-08-14
K001113 2000-06-13
K000989 2000-06-08
K993484 2000-05-25
K000937 2000-05-25
K000938 2000-05-25
K000939 2000-05-04
K000940 2000-05-04

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