# K992819: Wand Plus

- Pathway: 510(k) (Traditional)
- Applicant: Spintech, Inc.
- Decided: May 11, 2000 after 265 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
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Wand™ computer controlled syringe: named in the summary without a submission number

## Most influential descendants
- K023722: Safetywand Disposable Handpiece (2003), 0 descendants of its own

## Indications for use
To inject local anesthetic agents subcutaneously or intramuscularly for dental applications.

Source page: https://510kreport.com/device/K992819
Methodology: https://510kreport.com/methodology