# K072030: Implant Center

- Pathway: 510(k) (Traditional)
- Applicant: Satelec - Acteon Group
- Decided: Nov 19, 2007 after 118 days
- Product code: DZI (Drill, Bone, Powered)
- Device class: 2
- Regulation: 21 CFR 872.4120
- 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 K020833 (2002). 2 ancestors in all.
12 later devices descend from it; 1 cites it directly.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K040529: Cocoon Hygienist, Satelec (2004) Summary page 1.

## Most influential descendants
- K091252: Implant Center 2 (2009), 11 descendants of its own
- K100410: Piezoelectric System (2010), 8 descendants of its own
- K132848: Piezosurgery Flex (2013), 6 descendants of its own
- K172464: XD880A Ultrasonic Osteotomy Surgical System (2018), 2 descendants of its own
- K153743: Piezosurgery Plus (2016), 2 descendants of its own

## Indications for use
The intended use of the Satelec Implant Center is to supply utilities to and serve as a base for dental tools and accessories for use by qualified dental practitioners.

Source page: https://510kreport.com/device/K072030
Methodology: https://510kreport.com/methodology