# K123386: Periotype X-Pert

- Pathway: 510(k) (Traditional)
- Applicant: Clinical House Europe GmbH
- Decided: Apr 26, 2013 after 175 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: 10 generations back to K894595 (1990). 28 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 30 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K050406: Nobelspeedy Implants, Nobel Biocare AB (2005) Summary page 1.
- K111581: 15 Esthetic Abutment Nobelactive 03.0 1.5MM, 15 Esthetic Abutment Nobelactive 03.0 3MM, 15 Esthetic Abutment Nobelactive, Nobel Biocare AB (2011) Summary page 1.
- K944962: Branemark System 17 Angulated Abutment, Nobelpharma USA, Inc. (1995) Summary page 1.
- K920452: The Branemark System Ball Attachment Abutment Syst, Nobelpharma USA, Inc. (1993) Summary page 1.
- K925779: Branemark System Titanium Healing Abutments, Nobelpharma USA, Inc. (1993) Summary page 2.

## Most influential descendants
- K151169: OsteoReady ZircoSeal Abutments (2015), 0 descendants of its own

## Indications for use
PerioType X-Pert Implants are threaded, root-form dental implants Intended for use in the upper and lower jaw to support prosthetic devices, such as artificial teeth, in order to restore aesthetics and chewing function to partially or fully edentulous patients. PerioType X-Pert Dental Implant Systems are indicated for delayed loading. The PerioType X-Pert Abutments are straight and angled dental implant Abutments to be used in conjunction With the PerioType X-Pert dental implant fixture to aid in prosthetic rehabilitation.

Source page: https://510kreport.com/device/K123386
Methodology: https://510kreport.com/methodology