# K981490: Willi Geller Creation Porcelain

- Pathway: 510(k) (Traditional)
- Applicant: Jensen Industries, Inc.
- Decided: Oct 22, 1998 after 178 days
- Product code: EIH (Powder, Porcelain)
- Device class: 2
- Regulation: 21 CFR 872.6660
- 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 K900209 (1990). 1 ancestor in all.
6 later devices descend from it; 4 cite it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K900209: Willi Geller Ceramic Creation & Surprise, Creation North America, Inc. (1990) Summary page 1.

## Most influential descendants
- K140848: Luminesse Porcelain System (2014), 2 descendants of its own
- K182350: Dental Ceramic (2019), 0 descendants of its own
- K163251: Life Essence Universal Porcelain System (2017), 0 descendants of its own
- K063842: Cyrtina System (2007), 0 descendants of its own
- K042638: Radiance Porcelain (2004), 0 descendants of its own

## Indications for use
The product is intended for use in fabricating oral crowns and bridges and laminate veneers and inlays for dental use.

Source page: https://510kreport.com/device/K981490
Methodology: https://510kreport.com/methodology