# K061904: Compudent Sta

- Pathway: 510(k) (Traditional)
- Applicant: Milestone Scientific, Inc.
- Decided: Aug 8, 2006 after 34 days
- Product code: EJI (Syringe, Cartridge)
- Device class: 2
- Regulation: 21 CFR 872.6770
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device 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) CompuDent computer controlled syringe: named in the summary without a submission number

## Recalls of this device
- Feb 11, 2015 · Class III · Z-1952-2015: Wand Handpiece was mislabeled as STA handpiece. The Wand handpiece cannot be installed in the STA instrument.

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

Source page: https://510kreport.com/device/K061904
Methodology: https://510kreport.com/methodology