# K072830: RM Bond, Model J032

- Pathway: 510(k) (Traditional)
- Applicant: Pentron Clinical Technologies
- Decided: Dec 4, 2007 after 62 days
- Product code: DYH (Adhesive, Bracket And Tooth Conditioner, Resin)
- Device class: 2
- Regulation: 21 CFR 872.3750
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K020394 (2002). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K020394: Apc Plus Adhesive, 3M Unitek (2002) Summary page 1.

## Indications for use
RM Bond Adhesive product is indicated for orthodontic appliance applications using an indirect bonding treatment technique.

Source page: https://510kreport.com/device/K072830
Methodology: https://510kreport.com/methodology