# K123929: Begopal+

- Pathway: 510(k) (Abbreviated)
- Applicant: Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO
- Decided: Mar 14, 2013 after 84 days
- Product code: EJH (Alloy, Metal, Base)
- Device class: 2
- Regulation: 21 CFR 872.3710
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K032136 (2003). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K032136: Wirobond C, Bego U.S.A. (2003) Summary page 1.
- (no number) Wirobond C+ (510(k) exempt): named in the summary without a submission number
- (no number) Callisto CP+ (510(k) exempt): named in the summary without a submission number

## Indications for use
BegoPal+ is a porcelain-fused-to-metal (PFM) noble alloy. It is suitable for fabrication of crown and bridge restorations. BegoPal+ is available as powder and is processed by selective laser melting.

Source page: https://510kreport.com/device/K123929
Methodology: https://510kreport.com/methodology