# K983786: Sterngold Implamed Wide Platform Dental Implants and Related Prosthetics and Insttumentation

- Pathway: 510(k) (Special)
- Applicant: Sterngold/Implamed
- Decided: Nov 13, 1998 after 17 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
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Indications for use
The Sterngold ImplaMed Implant can be used in dental implant applications for oral rehabilitation of edentulous and partially dentate patients in the maxilla and mandible. Implant retained restorations may consist of single crowns or bridges as well as complete or patrtial dentures.

Source page: https://510kreport.com/device/K983786
Methodology: https://510kreport.com/methodology