Diazyme

Catalogue number DZ168C-KY1, listed by Diazyme Laboratories, Inc., United States, under Assay, Glycosylated Hemoglobin. 3 manufacturers in China are registered for this product code.

Registry build 21.09.26
3manufacturers in China registered for this device type
1catalogue number
5510(k) clearances naming this product code

Who Else Makes It

Concentrated in Shanghai (2), Jiangsu (1).

Chinese manufacturers registered for FDA product code LCP
Manufacturer City Province Registered as Device types
Wuxi Biohermes BIO & Medical Technology Co., Ltd. Wuxi Jiangsu Manufacturer 3
Shanghai Medconn Medical Technology Co., Ltd. Shanghai Shanghai Manufacturer 2
Shanghai Medconn Biotechnology Co., Ltd. Jinshan District Shanghai Manufacturer 2

Record

Regulatory record for Diazyme
Listed by Diazyme Laboratories, Inc., United States
FDA product code LCP
Device type Assay, Glycosylated Hemoglobin
Device class Class 2
Regulation 21 CFR 864.7470
Establishment Specification developer, Repacker / relabeller, Manufacturer
510(k) K160762
Record published 2020-07-21
Record revised 2026-01-21 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied as a kit Yes
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for Diazyme
Catalogue number Size Status
DZ168C-KY1 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Trinity Biotech Primus Corp. 36
Variant II Turbo Bio-Rad Laboratories Inc. 15
Pointe Scientific, Inc. Horiba Instruments Incorporated 11
Variant II Turbo Link Bio-Rad Laboratories Inc. 7
D-10 Bio-Rad Laboratories Inc. 7
Variant II Hemoglobin A1c Bio-Rad Laboratories Inc. 5
Drew Scientific Drew Scientific, Ltd. 5
Tosoh Automated Glycohemoglobin Analyzer HLC-723GR01 Tosoh Corp. 4
D-100 Bio-Rad Laboratories Inc. 4
Fructosamine Roche Diagnostics Gmbh 4
D-10 Dual Bio-Rad Laboratories Inc. 3
JAS Diagnostics Drew Scientific, Ltd. 3

Showing 12 of 134. All products under Assay, Glycosylated Hemoglobin

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K160762 2016-11-21
K133803 2014-08-06
K110188 2011-05-17
K070734 2007-04-09
K042193 2004-10-29

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