# K150669: Neoss TiBase, Neoss CoCr Abutments (Mono and Multi)

- Pathway: 510(k) (Traditional)
- Applicant: Neoss, Ltd.
- Decided: Oct 8, 2015 after 206 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: 3 generations back to K891615 (1989). 7 ancestors in all.
14 later devices descend from it; 2 cite it directly.
0 of 22 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K043195: Neo Implant System, Neoss, Ltd. (2005) Summary page 6.

## Most influential descendants
- K163634: External Hex Implants (2017), 13 descendants of its own
- K193084: TIB Abutment System (2020), 3 descendants of its own
- K183024: Implacil Implant System (2020), 2 descendants of its own
- K180465: Provata Implant System (2018), 2 descendants of its own
- K231967: ARi ExCon Implant System (2023), 1 descendant of its own

## Indications for use
Neoss Abutments are designed to be connected to the Neoss Implants and intended for use as an aid in prosthetic rehabilitation. The Neoss TiBase is compatible with the Sirona Dental System inCoris ZI Meso L. All digitally designed copings and/or crowns for use with the Neoss TiBase Abutments are to be designed and milled using the Sirona Dental CAD/CAM System. Neoss abutments are designed to be connected to the Neoss Implants and intended for use as an aid in prosthetic rehabilitation.

Source page: https://510kreport.com/device/K150669
Methodology: https://510kreport.com/methodology