# K032455: Panavia F 2.0

- Pathway: 510(k) (Traditional)
- Applicant: Kuraray Medical, Inc.
- Decided: Nov 7, 2003 after 88 days
- Product code: EMA (Cement, Dental)
- Device class: 2
- Regulation: 21 CFR 872.3275
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K931812 (1993). 18 ancestors in all.
34 later devices descend from it; 14 cite it directly.
0 of 53 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K012432: Modification to Clearfil Photo Bond, Kuraray Medical, Inc. (2001)
- K012442: Modification to Clearfil SE Bond, Kuraray Medical, Inc. (2001)

## Most influential descendants
- K094007: Unicem (2010), 22 descendants of its own
- K100756: MALTA (2010), 19 descendants of its own
- K062410: Clearfil Esthetic Cement & DC Bond (2006), 10 descendants of its own
- K081583: Clearfil SA Cement (2008), 9 descendants of its own
- K110508: Suglue-10 (2011), 8 descendants of its own

## Indications for use
PANAVIA F 2.0 is indicated for the following applications: Cementation of metal crowns and bridges, inlays and onlays. Cementation of porcelain crowns, inlays and onlays and veneers. Cementation of composite resin crowns, inlays and onlays Cementation of adhesion bridges Cementation of endodontic cores and prefabricated posts Amalgam bonding

Source page: https://510kreport.com/device/K032455
Methodology: https://510kreport.com/methodology