Aliquot

Syringe Delivery Kit

Registry build 21.09.26
3manufacturers in China registered for this device type
1catalogue number
1recall

Who Else Makes It

Concentrated in Jiangsu (2), Guangdong (1).

Chinese manufacturers registered for FDA product code KIH
Manufacturer City Province Registered as Device types
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Jiangsu Changmei Medtech Co., Ltd. Changzhou Jiangsu Contract manufacturer 8
Guangzhou Clean Medical Products Manufacturing Corp Guangzhou Guangdong Contract manufacturer 5

Record

Regulatory record for Aliquot
Listed by Stryker GmbH, Switzerland
FDA product code KIH
Device type Dispenser, Cement
Device class Class 1
Regulation 21 CFR 888.4200
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer
Premarket notification Exempt
Record published 2017-12-20
Record revised 2025-09-22 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number, expiry date
Storage Storage environment temperature 20 to 30 °C
Sizes Length 10 cm; needle gauge 11 G
Distribution end date 2025-09-22

Catalogue Numbers

Catalogue numbers for Aliquot
Catalogue number Size Status
2090-0501 Length 10.0 cm Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Dispenser, Cement Medtronic Sofamor Danek, Inc. 14
Pressurizer Adler Ortho SpA 11
DJO Surgical Encore Medical, L.P. 7
Vortex Smith & Nephew, Inc. 6
Dispenser, Cement Zimmer, Inc. 5
Miller™ Zimmer, Inc. 5
Dispenser, Cement Synthes (U.S.A.) LP 5
SpineJack Stryker GmbH 4
Kyphon® Cement Delivery System Medtronic Sofamor Danek, Inc. 4
Medtronic Reusable Instruments Medtronic Sofamor Danek, Inc. 4
PowerFlo Zimmer, Inc. 4
Palamix® Heraeus Medical LLC 3

Showing 12 of 111. All products under Dispenser, Cement

Recalls

The FDA has not published a severity grade for these. 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
2012-01-13 Not classified Mixed-up of materials/components The firm identified two complaints have been reported indicating that the product inside the package did not match with the label information. The product was labeled as Flat Proximal Pressurizer P/N 0206-556-000 while the product inside th 10 boxes (60 units) 2013-07-24

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