# K052741: Implantmed SI-915 (115V Version); Implantmed SI-923 (230V Version) Incl. Accessories

- Pathway: 510(k) (Traditional)
- Applicant: W&H Dentalwerk Buermoos GmbH
- Decided: Jan 13, 2006 after 105 days
- Product code: EBW (Controller, Foot, Handpiece And Cord)
- Device class: 1
- Regulation: 21 CFR 872.4200
- 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 K002469 (2001). 1 ancestor in all.
27 later devices descend from it; 8 cite it directly.
0 of 29 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K002469: Implantmed SI-95 115 (100-130 V) and SI-95 230 (220-240 V), W&H Dentalwerk Buermoos GmbH (2001) Summary page 1.

## Most influential descendants
- K161957: W&H Implantmed SI-1015 incl. Accessories (2016), 8 descendants of its own
- K173905: Surgic Pro, Surgic Pro+ (2018), 5 descendants of its own
- K123695: Traus SIP10 (2012), 4 descendants of its own
- K092214: Chiropro L System (2009), 4 descendants of its own
- K080939: Surgical Handpieces, Mikro Saw Handpieces (2008), 3 descendants of its own

## Indications for use
Mechanical drive unit with coolant supply for transmission instruments with coupling system according to ISO 3964. The equipment is a drive unit for use in dental surgery, implantology, maxillo-facial surgery and endodontics for treatment of dental hard tissue and mechanical rotating root canal preparation

Source page: https://510kreport.com/device/K052741
Methodology: https://510kreport.com/methodology