Vitros

VITROS Chemistry Products LAC Slides

Registry build 21.09.26
3manufacturers in China registered for this device type
2catalogue numbers in this listing
3recalls on this code

Who Else Makes It

Concentrated in Shandong (1), Hunan (1), Jiangsu (1).

Chinese manufacturers registered for FDA product code KHP
Manufacturer City Province Registered as Device types
Biobase Biodustry(Shandong)Co., Ltd. Jinan Shandong Manufacturer 70
AVE Science & Technology Co., Ltd. Changsha Hunan Manufacturer 22
Eaglenos Sciences, Inc. Nanjing Jiangsu Manufacturer 4

Record

Regulatory record for Vitros
Listed by Ortho-Clinical Diagnostics, Inc., United States
FDA product code KHP
Device type Acid, Lactic, Enzymatic Method
Device class Class 1
Regulation 21 CFR 862.1450
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Premarket notification Exempt
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 -18 to -18 °C

Catalogue Numbers

Catalogue numbers for Vitros
Catalogue number Size Status
8150112 In distribution
8433880 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
StatSensor/StatStrip Nova Biomedical Corporation 5
Stat Profile Nova Biomedical Corporation 5
Lactate Gen.2 Roche Diagnostics Gmbh 4
Lactate Plus Nova Biomedical Corporation 4
Biobase Biobase Biodustry(Shandong)Co., Ltd. 3
i-STAT Abbott Point OF Care Inc. 3
Alinity Abbott Medical 2
Fora Fora Care Inc. 2
LA Cartridge LifeHealth, LLC 2
L-Lactate (LAC) Randox Laboratories Limited 2
ABX Pentra Lactic Acid Horiba ABX SAS 1
Alinity Abbott Ireland 1

Showing 12 of 43. All products under Acid, Lactic, Enzymatic Method

Recalls Naming This Product

1 recall names this product by its own identifier, the UDI on its label.

Recalls naming the identifiers of Vitros
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Ortho-Clinical Diagnostics, Inc. UDI-DI 2025-07-29 Class II Device Design VITROS Chemistry Products LAC Slides on VITROS XT 3400 and VITROS XT 7600 Systems are experiencing an increased occurrence of calibration failure related to lots from coating 0130 and above with Condition Code TH4-63J during calibration, ca 2,320 units

Recalls

2 of these are Class II. 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
2025-07-29 Class II Device Design VITROS Chemistry Products LAC Slides on VITROS XT 3400 and VITROS XT 7600 Systems are experiencing an increased occurrence of calibration failure related to lots from coating 0130 and above with Condition Code TH4-63J during calibration, ca 2,908 units
2016-08-11 Class II Under Investigation by firm Ortho Clinical Diagnostics confirmed that N-Acetylcysteine (NAC), a drug used for acetaminophen overdose, mucolytic therapy and is used as nutritional supplement, can interfere with VITROS GLU, LAC, TRIG, and URIC Slides assays. US: 32,081 sales units; Foreign: 29,932 sales units 2018-06-11

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