# K112333: LRT Attachment

- Pathway: 510(k) (Traditional)
- Applicant: Bcf Certification, Inc.
- Decided: Jan 30, 2012 after 171 days
- Product code: NHA (Abutment, Implant, Dental, Endosseous)
- Device class: 2
- Regulation: 21 CFR 872.3630
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K934668 (1994). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K994257: Locator Implant Anchor, Zest Anchors, Inc. (2000) Summary page 1.
- K955372: Ball Attachment System, Nobelpharma USA, Inc. (1996) Summary page 1.

## Cited in the summary but kept off the family tree
- K0001638: 0-ring Prosthetic Attachment. Number could not be read

## Indications for use
The LRT Attachment System is indicated for providing a mean of attaching a removable prosthetic device to an endosseous implant body.

Source page: https://510kreport.com/device/K112333
Methodology: https://510kreport.com/methodology