# K002168: Aspiject Self-Aspirating Dental Injection Syringe

- Pathway: 510(k) (Abbreviated)
- Applicant: Ronvig Instruments, Ltd.
- Decided: Oct 13, 2000 after 88 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.
4 later devices descend from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K040671: Eroject, Miniject, Self Aspirating Syringes, Aspirating Syringes, Non Aspirating Syringes (2004), 3 descendants of its own
- K083796: Miltex Aspirating Syringe, Miltex Petite Aspirating Syringe, Miltex Self-Aspirating Syringe, Miltex Lightweight (2009), 2 descendants of its own
- K171254: LeEject 2 Dental Syringe and Needle System (2017), 0 descendants of its own
- K092943: Aspirating Syringe, Non-Aspirating Syringe (2009), 0 descendants of its own

Source page: https://510kreport.com/device/K002168
Methodology: https://510kreport.com/methodology