# K980726: Ultra-Blaster

- Pathway: 510(k) (Traditional)
- Applicant: Ultradent Products, Inc.
- Decided: May 12, 1998 after 77 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
Ultra-Blaster 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 bridges. Sandblasting of porcelain and resin surfaces prior to bonding and replaces use of hydrofluric 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 endodontic posts prior to cementation. Sandblasting of all surfaces, to be bonded.

Source page: https://510kreport.com/device/K980726
Methodology: https://510kreport.com/methodology