# K121391: Inclusive Titanium Abutments for Camlog Screw-Line Implants

- Pathway: 510(k) (Traditional)
- Applicant: Prismatik Dentalcraft, Inc.
- Decided: Dec 10, 2012 after 215 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: 1 generation back to K073553 (2008). 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)
- K073553: Camlog Implant System Abutments, Altatec GmbH (2008) Summary page 1.

## Indications for use
The Inclusive Titanium Abutments for Camlog Screw-Line Implants are premanufactured prosthetic components directly connected to endosseous dental implants and are intended for use as an aid in prosthetic rehabilitation. They are compatible with the Camlog Screw-Line Implants in 3.3mm, 3.8mm, 4.3mm, 5.0mm and 6.0mm diameters.

Source page: https://510kreport.com/device/K121391
Methodology: https://510kreport.com/methodology