# K960548: AH Plus Root Canal Sealer

- Pathway: 510(k) (Traditional)
- Applicant: Dentsply Intl.
- Decided: Apr 26, 1996 after 78 days
- Product code: KIF (Resin, Root Canal Filling)
- Device class: 2
- Regulation: 21 CFR 872.3820
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
55 later devices descend from it; 11 cite it directly.
0 of 56 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) AH26® Root Canal Sealer: named in the summary without a submission number

## Most influential descendants
- K080917: Iroot SP (2008), 37 descendants of its own
- K082943: Iroot BP, Model Irbp 4609 (2009), 12 descendants of its own
- K992727: The BI-Directional Spiral & Epoxy Root Canal Cement System (2000), 9 descendants of its own
- K170175: Endoseal Mta (2018), 8 descendants of its own
- K092715: Iroot BP Plus (2009), 7 descendants of its own

## Indications for use
AH® PLUS™ Root Canal Sealer is used for permanent sealing of root canals following established endodontic procedures.

Source page: https://510kreport.com/device/K960548
Methodology: https://510kreport.com/methodology