# K003226: The Lifecore Stage-1 Single Stage RBM Dental Implant System

- Pathway: 510(k) (Traditional)
- Applicant: Lifecore Biomedical, Inc.
- Decided: Jan 12, 2001 after 88 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.
400 later devices descend from it; 5 cite it directly.
0 of 401 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K051576: Avana Dental Implant System (2005), 222 descendants of its own
- K062051: SS System (2006), 211 descendants of its own
- K063861: GS System (2007), 202 descendants of its own
- K062030: US System (2006), 183 descendants of its own
- K101945: Neodent Implant System (2011), 180 descendants of its own

Source page: https://510kreport.com/device/K003226
Methodology: https://510kreport.com/methodology