# K001730: GC Fujicem

- Pathway: 510(k) (Traditional)
- Applicant: GC America, Inc.
- Decided: Jul 17, 2000 after 40 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.
17 later devices descend from it; 3 cite it directly.
0 of 18 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
- K022476: Relyx Rmgip (2002), 15 descendants of its own
- K111185: Relyx Luting Plus Automix (2011), 10 descendants of its own
- K123265: Rmgi Low Viscosity (2012), 5 descendants of its own
- K130223: Rmgi Fill (2013), 4 descendants of its own
- K182854: GC FujiCEM 2 (Improved) (2019), 1 descendant of its own

Source page: https://510kreport.com/device/K001730
Methodology: https://510kreport.com/methodology