# K023722: Safetywand Disposable Handpiece

- Pathway: 510(k) (Traditional)
- Applicant: Spintech, Inc.
- Decided: Sep 2, 2003 after 301 days
- Product code: EJI (Syringe, Cartridge)
- Device class: 2
- Regulation: 21 CFR 872.6770
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K851903 (1985). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K992819: Wand Plus, Spintech, Inc. (2000) Summary page 1.
- K962999: Safety Injection System, Integritech, Inc. (1997) Summary page 1.

## Indications for use
The SafetyWand is intended to inject local anesthetic agents subcutaneously or intramuscularly for dental applications. It is a sterile single use handpiece assembly for use with the Milestone Compudent computer controlled injection system. The SafetyWand incorporates safety engineering sharps protection features to aid in the prevention of needlesticks.

Source page: https://510kreport.com/device/K023722
Methodology: https://510kreport.com/methodology