True Metrix

Good Neighbor Pharmacy True Metrix Self Monitoring Blood Glucose Meter - Free Meter Only

Registry build 21.09.26
20manufacturers in China registered for this device type
40catalogue numbers in this listing
2510(k) clearances naming this product code
13recalls on this code

Who Else Makes It

Concentrated in Guangdong (8), Jiangsu (4), Zhejiang (4). 8 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code NBW
Manufacturer City Province Registered as Device types
Acon Biotech (Hangzhou) Co., Ltd. Hangzhou Zhejiang Contract manufacturer 29
Sanmina Kunshan Jiangsu Contract manufacturer 15
Dongguan Honfield Precision Parts Co., Ltd. Zhangmutou, Dongguan Guangdong Contract manufacturer 8
Flextronics Medical Device Manufacturing (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 6
Flextronics Industrial (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 5
Yasee Biomedical Inc Qingdao Shandong Contract manufacturer 5
Altek Medical (kunshan) limited Kunshan Free Trade Zone Jiangsu Contract manufacturer 2
Dongguan Kaifa Technology Co., Ltd. Dongguan Guangdong Contract manufacturer 2
Jiangsu NEW Pentastar Medical Products Co., Ltd. Changzhou Jiangsu Exporter 146
Steris Sterilization Technologies (Suzhou) Ltd Suzhou Jiangsu Contract manufacturer 44
Andon Health Co., Ltd. Tianjin Tianjin Contract manufacturer 22
Vivachek Biotech (Hangzhou) Co., Ltd. Hangzhou, Zhuji Zhejiang Contract manufacturer 21

Showing 12 of 20. All 20 manufacturers in China registered for System, Test, Blood Glucose, Over The Counter

Record

Regulatory record for True Metrix
Listed by Trividia Health, Inc., United States
FDA product code NBW
Device type System, Test, Blood Glucose, Over The Counter
Device class Class 2
Regulation 21 CFR 862.1345
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
Record published 2016-09-20
Record revised 2025-11-13 (version 18)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Over the counter Yes
Supplied as a kit Yes
Label carries lot or batch number, expiry date, serial number
Storage Storage environment temperature 40 to 86 °F
Packaging Case of 12, box, case of 24, case of 4, case of 40, box of 2
Distribution end date 2024-08-28

Catalogue Numbers

Catalogue numbers for True Metrix
Catalogue number Size Per pack Status
TRUE METRIX SELF MONITORING BLOOD GLUCOSE METER In distribution
TRUE METRIX Self Monitoring Blood Glucose Meter In distribution
TRUE METRIX PRE-PACK 4×24 In distribution
TRUE METRIX SELF MONITORING BLOOD GLUCOSE METER In distribution
TRUE METRIX Self Monitoring Blood Glucose Meter In distribution
TRUE METRIX SELF MONITORING BLOOD GLUCOSE METER – NOT FOR RETAIL SALE In distribution
TRUE METRIX self monitoring blood glucose meter In distribution
TRUE METRIX Self Monitoring Blood Glucose Meter Kit In distribution
TRUE METRIX SELF MONITORING BLOOD GLUCOSE METER – FREE METER ONLY In distribution
TRUE METRIX Self Monitoring Blood Glucose Meter In distribution
TRUE METRIX Self Monitoring Blood Glucose Meter In distribution
TRUE METRIX SELF MONITORING BLOOD GLUCOSE METER – NOT FOR RETAIL SALE In distribution
TRUE METRIX Self-Monitoring Blood Glucose Meter In distribution
TRUE METRIX SELF MONITORING BLOOD GLUCOSE METER In distribution
TRUE METRIX PRE-PACK In distribution
TRUE METRIX self monitoring blood glucose meter In distribution
TRUE METRIX PRE-PACK 4×24 In distribution
TRUE METRIX Self Monitoring Blood Glucose Meter In distribution
TRUE METRIX self monitoring blood glucose meter In distribution
TRUE METRIX Self Monitoring Blood Glucose Meter → FREE METER ONLY In distribution
TRUE METRIX SELF MONITORING BLOOD GLUCOSE TEST STRIPS – 30 Test Strips 30 In distribution
TRUE METRIX SELF MONITORING BLOOD GLUCOSE METER In distribution
TRUE METRIX PRE-PACK 4×24 In distribution
TRUE METRIX SELF MONITORING BLOOD GLUCOSE METER – FREE METER ONLY In distribution
TRUE METRIX Self Monitoring Blood Glucose Meter In distribution
TRUE METRIX SELF MONITORING BLOOD GLUCOSE METER In distribution
TRUE METRIX PRE-PACK Withdrawn
TRUE METRIX SELF MONITORING BLOOD GLUCOSE METER Withdrawn
sunmark TRUE METRIX SELF MONITORING BLOOD GLUCOSE METER Withdrawn
TRUE METRIX SELF MONITORING BLOOD GLUCOSE METER – FREE METER ONLY Withdrawn
TRUE METRIX SELF MONITORING BLOOD GLUCOSE METER Withdrawn
TRUE METRIX self monitoring blood glucose meter Withdrawn
TRUE METRIX Self Monitoring Blood Glucose Meter Withdrawn
TRUE METRIX PRE-PACK 4×24 Withdrawn
TRUE METRIX SELF MONITORING BLOOD GLUCOSE METER Withdrawn
TRUE METRIX PRE-PACK 4×24 Withdrawn
TRUE METRIX PRE-PACK Withdrawn
TRUE METRIX SELF MONITORING BLOOD GLUCOSE METER Withdrawn
TRUE METRIX self monitoring blood glucose meter – FREE METER ONLY Withdrawn
TRUE METRIX PRE-PACK 4×24 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Fora Fora Care Inc. 31
True Metrix AIR Trividia Health, Inc. 21
GE Bionime Corporation 21
TRUEtrack Trividia Health, Inc. 17
Medline Medline Industries, Inc. 15
AgaMatrix Agamatrix 15
Tenovi Tenovi Co 13
Auvon Shenzhen Yuwen E-Commerce Co., Ltd. 11
Accu-Chek Guide Roche Diagnostics Operations 10
Curaplex Bound Tree Medical, LLC 10
OneTouch Verio Lifescan Europe Gmbh 10
Rightest Bionime Corporation 9

Showing 12 of 476. All products under System, Test, Blood Glucose, Over The Counter

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K262116 2026-07-23
K143548 2016-04-01

Recalls Naming This Product

2 recalls name this product by its own identifiers, the UDI on its label.

Recalls naming the identifiers of True Metrix
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Trividia Health, Inc. UDI-DI 2026-02-06 Class I Software design The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code description and recommended actions for the E-5 error code in the labeling do not: (a) clea 12,067,458
Trividia Health, Inc. UDI-DI 2025-10-07 Class II Device Design Manufacturing defect causing LCD display issues with missing or partial segments (ghosting) that can result in misreading glucose values, potentially leading to inappropriate treatment decisions for diabetes management. 601 units

Recalls

3 of these are Class I. Class I is the FDA’s most serious grade: a reasonable probability of serious injury or death. Class II means a temporary or reversible health consequence. 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
2026-02-06 Class I Software design The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code description and recommended actions for the E-5 error code in the labeling do not: (a) clea 3,678,026
2026-02-06 Class I Software design The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code description and recommended actions for the E-5 error code in the labeling do not: (a) clea 1,001,534
2026-02-06 Class I Software design The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code description and recommended actions for the E-5 error code in the labeling do not: (a) clea 1,407,465
2020-04-20 Class II Process control One (1) TRUE METRIX AIR blood glucose meter distributed in the United States was packaged into a TRUE METRIX blood glucose meter kit and has an incorrect factory-set unit of measure; the meter displays glucose results in mmol/L rather than 1 unit 2021-06-01
2016-06-28 Class II Nonconforming Material/Component Product gives incorrect low blood glucose levels. 5,527,921 In total =4,621,639 strips & 393,808 kits domestic
2016-06-28 Class II Nonconforming Material/Component Product gives incorrect low blood glucose levels. 5,527,921 In total =4,621,639 strips & 393,808 kits domestic
2016-06-28 Class II Nonconforming Material/Component Product gives incorrect low blood glucose levels. 5,527,921 In total =4,621,639 strips & 393,808 kits domestic
2016-06-28 Class II Nonconforming Material/Component Product gives incorrect low blood glucose levels. 5,527,921 In total =4,621,639 strips & 393,808 kits domestic
2013-10-02 Class II Software design (manufacturing process) Manufactured with an incorrect factory set unit of measure. 501 2016-01-28
2013-10-02 Class II Software design (manufacturing process) Manufactured with an incorrect factory set unit of measure. 105 2016-01-28
2013-02-25 Class II Environmental control Meter kit outer boxes containing 10 ct. test strips state incorrect storage temperature range. 1,627 Kits 2013-07-08

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