# K000100: Camlog Rootform Implant System

- Pathway: 510(k) (Special)
- Applicant: Altatec Biotechnologies
- Decided: Jan 28, 2000 after 15 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.
16 later devices descend from it; 2 cite it directly.
0 of 17 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K110640: Atlantis Abutment for Camlog Implant, Duplicate Abutment, Later Abutment (2011), 9 descendants of its own
- K132881: Z5C (2014), 8 descendants of its own
- K160207: ATLANTIS ISUS Implant Suprastructures (2016), 5 descendants of its own
- K172668: W Zirconia Implants (2018), 4 descendants of its own
- K163350: Multibase Abutments EV and ATLANTIS Suprastructures (2017), 4 descendants of its own

Source page: https://510kreport.com/device/K000100
Methodology: https://510kreport.com/methodology