Henry Schein

Clinical Sand Blaster Hook-up Kit

Registry build 21.09.26
1manufacturer
7catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Registered in Guangxi.

Chinese manufacturers registered for FDA product code KOJ
Manufacturer City Province Registered as Device types
Guilin Woodpecker Medical Instrument Co., Ltd. Guilin Guangxi Manufacturer 25

Record

Regulatory record for Henry Schein
Listed by Henry Schein, Inc., United States
FDA product code KOJ
Device type Airbrush
Device class Class 2
Regulation 21 CFR 872.6080
510(k) K014249
Record published 2016-09-24
Record revised 2026-07-03 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Label carries lot or batch number, serial number
Storage Storage environment temperature 0 to 40 °C; Special storage condition: Keep Dry
Sizes Weight 21 to 1770 g
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Henry Schein
Catalogue number Size Per pack Status
9004192 Weight 83 g In distribution
1015624 Weight 23 g In distribution
1015623 Weight 21 g In distribution
9004171 Weight 1770 g In distribution
9004193 Weight 28 g 50 In distribution
1017004 Weight 215 g In distribution
1026937 250 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
AIR-Flow E.M.S. Electro Medical Systems S.A. 21
Etchmaster Reliance Orthodontic Products, Inc. 21
Etchmaster Groman Inc. 18
Johnson-Promident Young Innovations Inc. 11
Jetpolisher 2000 Deldent, Ltd. 10
HuFriedyGroup HU-Friedy MFG Co., LLC 8
Microetcher Danville Materials, LLC 7
AIR-Flow-Piezon E.M.S. Electro Medical Systems S.A. 5
PWR Handpiece HU-Friedy MFG Co., LLC 3
CoJet™ Prep 3M Deutschland GmbH 2
JP/JST/JS Handpiece Deldent, Ltd. 2
GBT Machine Wireless Pedal E.M.S. Electro Medical Systems S.A. 2

Showing 12 of 48. All products under Airbrush

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K862384 1986-11-07

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