DIAGNODENT MANUFACTURED BY KAVO AMERICA

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Request for Information Form	Contact Information
Company Name	KAVO AMERICA
Address	340 EAST MAIN ST.
City, State, Zip	LAKE ZURICH, IL 60047
Country	US
FDA Owner/Operator Phone	202-828-0850
FDA Medical Specialty Code	DE - Dental
FDA Product Code	NBL
FDA Classification Name	LASER,FLUORESCENCE CARIES DETECTION
FDA Device Classification Code	Standards
FDA Regulation Number	872.1745
FDA Common Generic Name	VARIOUS
FDA Proprietary Device Name	DIAGNODENT
FDA Owner / Operator Number	9061616
FDA Owner / Operator Name	DANAHER CORPORATION
FDA Establishment Registration Number	1419798
FDA Registered Establishment Name	KAVO AMERICA
FDA Operation Code(s)	MM - Manufacturer
FDA Listing Date	03-20-00
FDA Listing Status Code	Active
Differentiation	N/A
Keywords	N/A
Description	N/A
Brochure	N/A
Product Website	N/A

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1	DENTSPLY PROFESSIONAL 1301 SMILE WAY YORK, PA 17404 US 717-849-4229 / 717-845-7511 4229	D-CARIES/DETECTAR	LASER FLUORESCENCE CARIES DETECTION DEVICE
2	INSPEKTOR DENTAL CARE BV QUELLIJNSTRAAT 92 AMSTERDAM, 1072 XX NL / 31-20-6764988	INSPEKTOR PRO, QLF DENTAL EXAMINATION DEVICE	DENTAL FLUORESCENCE EXAMINATION SYSTEM
3	NEKS TECHNOLOGIES, INC. 2816, J.A. BOMBARDIER LAVAL, QUEBEC, H7P 6E2 CA 450-973-3598 / 919-598-8666	MINI DETECTAR (TM), MINI DUO (TM), DUO (TM)	DENTAL CARIES/CALCULUS DETECTION DEVICE