# K130436: Multilink Hybrid Abutment Cement

- Pathway: 510(k) (Traditional)
- Applicant: Ivoclar Vivadent, AG
- Decided: Aug 20, 2013 after 180 days
- Product code: EMA (Cement, Dental)
- Device class: 2
- Regulation: 21 CFR 872.3275
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K090704 (2009). 1 ancestor in all.
5 later devices descend from it; 2 cite 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)
- K090704: Multilink Implant, Ivoclar Vivadent, Inc. (2009) Summary page 1.

## Most influential descendants
- 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
- K222457: Provata Implant System (2023), 0 descendants of its own

## Indications for use
Extraoral, permanent cementation of ceramic structures made of lithium dislicate glass ceramic (L52) or zirconium oxide on titaniumltitanium alloy or zirconium oxide bases.

Source page: https://510kreport.com/device/K130436
Methodology: https://510kreport.com/methodology