# K040891: KLS Martin Ortho Anchorage System (Plates)

- Pathway: 510(k) (Traditional)
- Applicant: KLS-Martin L.P.
- Decided: May 28, 2004 after 53 days
- Product code: DZE (Implant, Endosseous, Root-Form)
- Device class: 2
- Regulation: 21 CFR 872.3640
- 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 K925771 (1993). 8 ancestors in all.
7 later devices descend from it; 5 cite it directly.
0 of 16 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K944565: KLS-Martin Micro Osteosythesis System (1.5MM), KLS-Martin L.P. (1994) Summary page 1.
- K980460: Onplant Orthodontic System, Nobel Biocare Uas, Inc. (1998) Summary page 1.

## Most influential descendants
- K241314: KLS Martin Oral-Max Implants MR Conditional (bundled) (2024), 1 descendant of its own
- K091051: Bollard Miniplate Skeletal Anchorage System (2009), 1 descendant of its own
- K260137: KLS Martin IPS Oral-Max Implants - MR Conditional; Individual Patient Solutions - Ti (IPS-Ti); Individual Patient Solutions - PEEK (IPS-PEEK); KLS Martin Individual Patient Solutions (2026), 0 descendants of its own
- K173623: Anchor plate (2018), 0 descendants of its own
- K063473: Synthes Orthodontic Bone Anchor System (2007), 0 descendants of its own

## Indications for use
The KLS-Martin Ortho Anchorage System (Plates) are implants intended to be surgically placed in the mouth for use as an anchor for orthodontic procedures in patients.

Source page: https://510kreport.com/device/K040891
Methodology: https://510kreport.com/methodology