# K152247: ATLANTIS Crown

- Pathway: 510(k) (Traditional)
- Applicant: Dentsply International, Inc.
- Decided: Jan 29, 2016 after 172 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: 3 generations back to K013230 (2001). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K112152: Cercon HT, Dentsply International, Inc. (2011) Summary page 4.

## Indications for use
The ATLANTIS™ Crown is intended for use with an ATLANTIS™ Abutment and an endosseous implant to function as a substructure that also serves as the final restoration, in a partially or completely edentulous patient.

Source page: https://510kreport.com/device/K152247
Methodology: https://510kreport.com/methodology