# K001494: Modification to Prompt L-Pop

- Pathway: 510(k) (Traditional)
- Applicant: Espe Dental AG
- Decided: Jul 7, 2000 after 56 days
- Product code: KLE (Agent, Tooth Bonding, Resin)
- Device class: 2
- Regulation: 21 CFR 872.3200
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
44 later devices descend from it; 3 cite it directly.
0 of 45 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K020946: Adper Prompt (2002), 42 descendants of its own
- K040857: Modification to Adper Prompt (2004), 39 descendants of its own
- K060684: Adper Prompt, Adper Prompt L-Pop (2006), 38 descendants of its own
- K043043: Hermes Bond 2 (2005), 37 descendants of its own
- K071131: UNO (2007), 35 descendants of its own

Source page: https://510kreport.com/device/K001494
Methodology: https://510kreport.com/methodology