Synchron

Hemoglobin A1c Reagent (HbA1c- 400)

Registry build 21.09.26
3manufacturers in China registered for this device type
2catalogue numbers in this listing
5510(k) clearances naming this product code
1recall

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 Synchron
Listed by Beckman Coulter, Inc., United States
FDA product code LCP
Device type Assay, Glycosylated Hemoglobin
Device class Class 2
Regulation 21 CFR 864.7470
Establishment Contract manufacturer, Specification developer, Manufacturer, Exporter
Record published 2016-08-24
Record revised 2023-08-28 (version 4)

Specifications

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

Catalogue Numbers

Catalogue numbers for Synchron
Catalogue number Size Status
A87905 In distribution
B36415 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
K140829 2014-07-14
K120199 2012-10-12
K121492 2012-09-11
K042459 2004-11-17
K010748 2001-07-10

Recalls

The FDA has not published a severity grade for these. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2011-03-01 Not classified Pending The recall was initiated because Beckman Coulter has identified a problem with two lots of HbA1c APT reagent OSR61177.
When HbA1c APT reagent lots 9390 and 9472 are calibrated with HbA1c calibrator ODR3032,
elevated recovery may be observed
373 kits 2012-06-28

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