Vitros

VITROS Chemistry Products dTIBC Reagent

Registry build 21.09.26
2manufacturers in China registered for this device type
1catalogue number
2510(k) clearances naming this product code
2recalls on this code

Who Else Makes It

Concentrated in Jilin (1), Shandong (1).

Chinese manufacturers registered for FDA product code JMO
Manufacturer City Province Registered as Device types
Dirui Industrial Co., Ltd. Changchun Jilin Contract manufacturer 84
Biobase Biodustry(Shandong)Co., Ltd. Jinan Shandong Manufacturer 70

Record

Regulatory record for Vitros
Listed by Ortho-Clinical Diagnostics, Inc., United States
FDA product code JMO
Device type Ferrozine (Colorimetric) Iron Binding Capacity
Device class Class 1
Regulation 21 CFR 862.1415
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2020-04-18
Record revised 2023-06-21 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, expiry date
Storage Storage environment temperature 2 to 8 °C
Packaging Case of 36

Catalogue Numbers

Catalogue numbers for Vitros
Catalogue number Size Status
6802001 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Synermed® Infrared Laboratory Systems LLC 5
Fe Randox Laboratories Limited 4
Uibc-SL Sekisui Diagnostics, LLC 4
Biobase Biobase Biodustry(Shandong)Co., Ltd. 3
Synchron Beckman Coulter, Inc. 3
Total Iron-Binding Capacity 2 (TIBC_2) Randox Laboratories Limited 3
Iron (Total) Sekisui Diagnostics, LLC 2
Pointe Scientific, Inc. Horiba Instruments Incorporated 2
K-Assay® Uibc Reagent Kamiya Biomedical Company LLC 2
Total-Iron Binding Capacity (Tibc) Randox Laboratories Limited 2
Iron (Fe) Randox Laboratories Limited 2
Direct Tibc Reagent Medtest DX 1

Showing 12 of 29. All products under Ferrozine (Colorimetric) Iron Binding Capacity

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K061464 2006-06-15
K052867 2005-12-23

Recalls

2 of these are Class III. 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
2024-05-14 Class III Labeling design Kit assigned an extended expiration date of 24-Jul-2025 during release. The correct expiration date for Lot 2953 is 24-Jul-2024. If used past its true expiration and the customer does not have their Assay Data Disk (ADD) updated, the syste 1718
2016-05-24 Class III Nonconforming Material/Component Ortho Clinical Diagnostics started receiving customer complaints for biased results when using VITROS dTIBC Reagent GEN 30 product. Ortho’s investigation confirmed that incorrect calibration mathematics were assigned to the Calibrator Kit 2 US: 1517; Foreign: 842 2018-06-08

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