# K112152: Cercon HT

- Pathway: 510(k) (Traditional)
- Applicant: Dentsply International, Inc.
- Decided: Nov 9, 2011 after 105 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: 2 generations back to K013230 (2001). 2 ancestors in all.
3 later devices descend from it; 3 cite it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K013230: Cercon Base, Degussa - Ney Dental, Inc. (2001) Summary page 1.
- K051462: Modification to: Cercon Base, Dentsply Intl. (2005) Summary page 1.

## Most influential descendants
- K241557: Cercon® yo ML (2024), 0 descendants of its own
- K152247: ATLANTIS Crown (2016), 0 descendants of its own
- K130184: Zenolux (2013), 0 descendants of its own

## Indications for use
Cercon® ht is indicated in the anterior and posterior segments for: * crowns * telescopic primary crowns * multi-unit bridges (with no more than two pontics between abutment crowns) Cercon® ht can be used as a substructure (framework) which is then veneered with a dental veneering ceramic or can be used for full-contour application (without veneering) as well. In the case of telescopic primary crowns' the substructure is not veneered.

Source page: https://510kreport.com/device/K112152
Methodology: https://510kreport.com/methodology