Cholestech LDX™

Cholestech LDX Lipid Profile GLU is a test cassette used with the Cholestech LDX Analyzer to measure total cholesterol, HDL cholesterol, triglycerides and glucose. Samples may be whole…

Registry build 21.09.26

Cholestech LDX Lipid Profile GLU is a test cassette used with the Cholestech LDX Analyzer to measure total cholesterol, HDL cholesterol, triglycerides and glucose. Samples may be whole blood collected by fingerstick or venipuncture.

Inside the cassette, plasma is separated from blood cells and directed to reaction pads. Enzymatic reactions produce colored dyes, which the analyzer measures by reflectance photometry.

Listed Item

Cholestech LDX™ Lipid Profile GLU

Calculated Lipid Values

Measured lipid values are used to calculate estimated LDL cholesterol, non-HDL cholesterol and the total cholesterol-to-HDL ratio. A magnetic stripe on the cassette carries calibration information used to convert reflectance readings into concentrations.

8manufacturers in China registered for this device type
2catalogue numbers in this listing
1510(k) clearance
4recalls on this code

Who Else Makes It

Concentrated in Guangdong (3), Zhejiang (2), Jiangsu (1). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code CGA
Manufacturer City Province Registered as Device types
Acon Biotech (Hangzhou) Co., Ltd. Hangzhou Zhejiang Contract manufacturer 29
Dongguan BAO Kang Dian ZI KE JI Limited Dongguan Guangdong Contract manufacturer 24
Flextronics Industrial (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 5
Yasee Biomedical Inc Qingdao Shandong Contract manufacturer 5
Jiangsu NEW Pentastar Medical Products Co., Ltd. Changzhou Jiangsu Exporter 146
Vivachek Biotech (Hangzhou) Co., Ltd. Hangzhou, Zhuji Zhejiang Contract manufacturer 21
Shenzhen Yuwen E-Commerce Co., Ltd. Shenzhen Guangdong Repacker / relabeller 19
Tianjin Empecs Medical Device Co., Ltd. Tianjin Tianjin Contract manufacturer 8

Record

Regulatory record for Cholestech LDX™
Listed by Alere San Diego, Inc., United States
FDA product code CGA
Device type Glucose Oxidase, Glucose
Device class Class 2
Regulation 21 CFR 862.1345
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer, Exporter
510(k) K223179
Record published 2023-12-20
Record revised 2026-03-13 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date
Storage Storage environment temperature 2 to 8 °C

Catalogue Numbers

Catalogue numbers for Cholestech LDX™
Catalogue number Size Status
97991 In distribution
97990 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
i-STAT Abbott Point OF Care Inc. 48
YSI Incorporated YSI Incorporated 34
Auvon Shenzhen Yuwen E-Commerce Co., Ltd. 28
Stat Profile Nova Biomedical Corporation 17
Fora Fora Care Inc. 13
TRUEtrack Trividia Health, Inc. 12
JAS Diagnostics Drew Scientific, Ltd. 11
StatStrip Nova Biomedical Corporation 9
Gluc-PAP Randox Laboratories Limited 8
Nova Primary Nova Biomedical Corporation 8
Synermed® Infrared Laboratory Systems LLC 7
Prodigy No Coding Blood Glucose Test Strips Prodigy Diabetes Care, LLC 7

Showing 12 of 215. All products under Glucose Oxidase, Glucose

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K223179 2023-09-20

Recalls

2 of these are Class II. Class II means a temporary or reversible health consequence. Class III is unlikely to cause harm at all → typically a labelling or documentation fault. 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
2024-03-01 Class II Labeling design There is a potential that the Cholestech LDX battery (an external battery pack available as an optional accessory to the Cholestech LDX Analyzer) may swell which could cause minor burns, cuts or abrasions, or low current electrical shock to 559 units
2022-06-24 Class II Device Design Cholesterol test cassettes package insert is to be updated with new bilirubin interference information because it was found that samples containing bilirubin, at concentrations greater than 2.0 mg/dL (conjugated) or 1.6 mg/dL (unconjugated) 436,990
2013-10-23 Class III Labeling Change Control Alere initiated a recall of Cholestech LDX Lipid Profile-GLU test cassettes, Catalog Number 10-991, Lot # 320167, becuase an incorrect lot number was printed on the outer 10 pack kit box label. The incorrect Lot # number printed was 321067. 3,621 kits 2014-09-25
2011-02-18 Not classified Pending The recall was initiated due to an issue related to an error in the encoding of calibration coefficients in the sample cassette that cause the Cholestech LDX analyzer to report glucose values as >500 mg/dL regardless of the true value of th 5,305 Boxes 2012-04-02

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P990026 2002-02-04 CYGNUS GLUCOWATCH AUTOMATIC GLUCOSE BIOGRAPHER Animas Corp.

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