# K001823: Linkmax

- Pathway: 510(k) (Traditional)
- Applicant: GC America, Inc.
- Decided: Aug 16, 2000 after 61 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
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
- K153231: G-Cem LinkForce, Dual Cure Activator, Try-In Paste, Multi Primer (2016), 5 descendants of its own
- K200798: G-Cem One (2020), 3 descendants of its own
- K254109: G-Cem Universal (2026), 0 descendants of its own
- K254063: iCEM Universal Plus (2025), 0 descendants of its own
- K251946: G aenial Universal Injectable II (2025), 0 descendants of its own

Source page: https://510kreport.com/device/K001823
Methodology: https://510kreport.com/methodology