# K020376: Ahl Generic Glass Ionomer Aesthetic Restorative

- Pathway: 510(k) (Traditional)
- Applicant: Advanced Healthcare, Ltd.
- Decided: Apr 9, 2002 after 64 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.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
Class V cavities (particularly erosion lesions). Class III cavities. Posterior cavities in deciduous teeth. ‘Sticky’ pits and fissures. Free-hand veneering. For use only by dental professional such as DDS or DMD. Not for use by general public or OTC. Labels will bear this caution.

Source page: https://510kreport.com/device/K020376
Methodology: https://510kreport.com/methodology