# K053155: Vimplant

- Pathway: 510(k) (Traditional)
- Applicant: Cybermed, Inc.
- Decided: Nov 23, 2005 after 9 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K954678 (1996). 8 ancestors in all.
63 later devices descend from it; 3 cite it directly.
0 of 72 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K033849: Simplant System, Materialise NV (2004) Summary page 1.
- K013878: Cybermed, Inc., V-Works, Cybermed, Inc. (2001) Summary page 1.

## Most influential descendants
- K070803: Invivodental (2007), 38 descendants of its own
- K123519: Invivo  Dental (2013), 24 descendants of its own
- K071636: Codiagnostix (R) 5.72 (2007), 21 descendants of its own
- K130724: Codiagnostix Implant Planning Software (2013), 15 descendants of its own
- K140713: Planmeca Romexis (2014), 14 descendants of its own

## Indications for use
The Vimplant is intended for use as a software interface for the transfer of imaging information from a CT scanner and also as a pre-operative software for simulation and evaluation dental implant placement and surgical treatment options.

Source page: https://510kreport.com/device/K053155
Methodology: https://510kreport.com/methodology