# K013969: Miniblaster

- Pathway: 510(k) (Traditional)
- Applicant: Deldent, Ltd.
- Decided: Jan 10, 2002 after 38 days
- Product code: KOJ (Airbrush)
- Device class: 2
- Regulation: 21 CFR 872.6080
- Recalls of this device: none
- 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. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
Miniblaster is an autoclavable clinical sandblaster for: Sandblasting of metal surfaces prior to cementation of crown and inlays, bridges, Maryland bridges. Sandblasting to remove residual cement from crowns and bridged. Sandblasting of porcelain and resin surfaces prior to bonding and replaces use of hydrofluoric acid for add-on repairs. Sandblasting of orthodontic bands removes cement and enhances bonding. Acrylic facings can be restored by sandblasting and using a direct metal adhesive. Sandblasting of all surfaces to be bonded.

Source page: https://510kreport.com/device/K013969
Methodology: https://510kreport.com/methodology