# K952122: V-Gnathos Plus

- Pathway: 510(k) (Traditional)
- Applicant: Metalor Dental USA Corp.
- Decided: Jun 6, 1995 after 32 days
- Product code: EJT (Alloy, Gold-Based Noble Metal)
- Device class: 2
- Regulation: 21 CFR 872.3060
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
4 later devices descend from it; 2 cite it directly.
0 of 5 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
- K012826: Bioporta G, Model 2052 (2001), 2 descendants of its own
- K023391: Bioporta G (2002), 0 descendants of its own
- K023392: Agc Special Alloy (2002), 0 descendants of its own
- K020347: Agc Speziallegierung (2002), 0 descendants of its own

Source page: https://510kreport.com/device/K952122
Methodology: https://510kreport.com/methodology