# K091252: Implant Center 2

- Pathway: 510(k) (Traditional)
- Applicant: Satelec
- Decided: Jul 22, 2009 after 84 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: 3 generations back to K020833 (2002). 3 ancestors in all.
11 later devices descend from it; 2 cite 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)
- K072030: Implant Center, Satelec - Acteon Group (2007) Summary page 1.

## Most influential descendants
- 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
- K112188: Piezotome Solo (2012), 1 descendant of its own

## Indications for use
The intended use of the Satelec Implant Center 2 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/K091252
Methodology: https://510kreport.com/methodology