Advanced Instruments Inserts, Small Volume, Package of 100 – OsmoPRO MAX

Inserts, Small Volume, Package of 100 - OsmoPRO MAX

Registry build 21.09.26
4manufacturers in China registered for this device type
1catalogue number
7510(k) clearances naming this product code
1recall

Who Else Makes It

Concentrated in Shandong (2), Guangdong (1), Shanghai (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code JJM
Manufacturer City Province Registered as Device types
Guangzhou Four E’s Scientific Co., Ltd. Guangzhou Guangdong Contract manufacturer 61
Infitek Co., Ltd. Shanghai Shanghai Manufacturer 49
Labpeak Co., Ltd. Jinan Shandong Manufacturer 43
Scitek Global Co., Ltd. Jinan Shandong Manufacturer 43

Record

Regulatory record for Advanced Instruments Inserts, Small Volume, Package of 100 – OsmoPRO MAX
Listed by Advanced Instruments, LLC, United States
FDA product code JJM
Device type Osmometer For Clinical Use
Device class Class 1
Regulation 21 CFR 862.2730
Establishment Contract manufacturer, Manufacturer
Premarket notification Exempt
Record published 2026-06-17

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Label carries lot or batch number, manufacturing date

Catalogue Numbers

Catalogue numbers for Advanced Instruments Inserts, Small Volume, Package of 100 – OsmoPRO MAX
Catalogue number Size Status
552923 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
FreezePoint® Freezing Point Osmometer ELITechGroup Inc 4
Multi-OSMETTE Precision Systems, Inc. 3
Micro-OSMETTE Precision Systems, Inc. 2
Advanced Instruments OsmoPRO Multi-Sample Micro-Osmometer Advanced Instruments, LLC 2
Osmette Sample Tubes, 30 ul Precision Systems, Inc. 2
Osmette III Precision Systems, Inc. 2
Osmette XL Precision Systems, Inc. 2
Advanced Instruments Model 3250 Single-Sample Osmometer Sample Tubes, Box of 500 Advanced Instruments, LLC 2
Osmette A Precision Systems, Inc. 2
Touch Micro-OSMETTE Precision Systems, Inc. 1
Multi-OSMETTE Carousel, Spare Precision Systems, Inc. 1
Micro-OSMETTE Sample Tubes, 50 ul Precision Systems, Inc. 1

Showing 12 of 60. All products under Osmometer For Clinical Use

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K965036 1997-02-20
K962056 1996-07-11
K925970 1993-07-09
K911092 1991-05-22
K873642 1987-10-20
K832783 1983-11-28
K790611 1979-06-15

Recalls

1 of these is 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
2024-03-11 Class II Under Investigation by firm System error messages may delay the ability to test patient samples and the need for frequent calibration due to results outside the expected range when testing controls. 58 units

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