# K092214: Chiropro L System

- Pathway: 510(k) (Traditional)
- Applicant: Bien-Air Dental, SA
- Decided: Dec 15, 2009 after 146 days
- Product code: EBW (Controller, Foot, Handpiece And Cord)
- Device class: 1
- Regulation: 21 CFR 872.4200
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K002469 (2001). 4 ancestors in all.
4 later devices descend from it; 2 cite it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K052741: Implantmed SI-915 (115V Version); Implantmed SI-923 (230V Version) Incl. Accessories, W&H Dentalwerk Buermoos GmbH (2006) Summary page 1.
- K970953: E-Type Speed Reducer Contra Angle, Nsk Nakanishi, Inc. (1997) Summary page 1.
- K011061: Surgical Contra-Angel Handpieces Types WS-56E,WS-75E/KM,WS-92 E/3,Surgical Straight Handpieces Types, S-9, S-10, S-11, W&H Dentalwerk Buermoos GmbH (2001)

## Most influential descendants
- K140308: Mastersurg / Expertsurg (2014), 2 descendants of its own
- K213139: SURGmatic S15 L Pro (2021), 0 descendants of its own
- K193341: iCTmotor (WL-1) (2020), 0 descendants of its own
- K102241: Anthogyr Implanteo Implantology and Dental Surgical Motor Unit (2011), 0 descendants of its own

## Recalls of this device
- Oct 24, 2013 · Class II · Z-0273-2014: The recall was initiated because there is a potential for malfunction of the OsseoCare Pro when used with the OseeoCare Pro iPad application software release 1.2.0.7.

## Indications for use
The Chiropro L system is intended for use in dental surgery, endlodontics, and implantology. The main unit is designed to be used with a specific dental micromnotor that drives dental handpieces fitted with appropriate tools to cut hard and soft tissues in the mouth and to screw dental implants.

Source page: https://510kreport.com/device/K092214
Methodology: https://510kreport.com/methodology