# K232740: Paltop Short Implants

- Pathway: 510(k) (Traditional)
- Applicant: Paltop Advanced Dental Solutions, Ltd.
- Decided: May 22, 2024 after 258 days
- Product code: DZE (Implant, Endosseous, Root-Form)
- Device class: 2
- Regulation: 21 CFR 872.3640
- 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 K071638 (2007). 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)
- K172576: BioHorizons Tapered Short Implants, BioHorizons Implant Systems, Inc. (2017) Summary page 5.

## Indications for use
Paltop Short Implants (Internal Hex and Conical Connections) are indicated for use in surgical and restorative applications for placement in the bone of the upper or lower jaw as an artificial root structure for single tooth replacement or for fixed bridgework to provide support for prosthetic devices, such as artificial teeth, in order to restore the patient’s chewing function. Paltop Short Implants are indicated to be used only with straight abutments and are for delayed loading only.

Source page: https://510kreport.com/device/K232740
Methodology: https://510kreport.com/methodology