# K090704: Multilink Implant

- Pathway: 510(k) (Traditional)
- Applicant: Ivoclar Vivadent, Inc.
- Decided: Jun 17, 2009 after 92 days
- Product code: EBF (Material, Tooth Shade, Resin)
- Device class: 2
- Regulation: 21 CFR 872.3690
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
6 later devices descend from it; 1 cites it directly.
0 of 7 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
- K130436: Multilink Hybrid Abutment Cement (2013), 5 descendants of its own
- K193084: TIB Abutment System (2020), 3 descendants of its own
- K240888: Calibra Abutment Resin Cement (2024), 0 descendants of its own
- K230873: Angulated Screw Channel (ASC) Solution Abutments & SI-BASE Abutments (2023), 0 descendants of its own
- K222469: TIB Abutments (2023), 0 descendants of its own

Source page: https://510kreport.com/device/K090704
Methodology: https://510kreport.com/methodology