Regulatory Compliance Information

ClaroNav is proud to report that it has achieved and maintains compliance with regulatory requirements throughout the world. Our products are designed and manufactured under our ISO 13485:2003 and FDA-compliant Quality Management System and our products are certified to all applicable standards. Please see the list below for our international registrations.

QUALITY MANAGEMENT SYSTEM

ISO 13485 quality system certification (PDF format)
ISO 13485:2003 certificate (ClaroNav)  ISO 13485:2003 certificate  (ClaroNav Kolahi Inc.)

US FDA Good Manufacturing Practice (GMP) 
We are fully compliant with 21 CFR Part 820, US FDA Quality Systems Regulations. View our Establishment Registration on the FDA website 

PRODUCT CERTIFICATIONS AND APPROVALS

AUSTRALIA – Devices listed in ARTG 
Navident 

CANADA – Medical Device Licenses 
Navident | NaviENT 

EUROPE – CE Marking certificates (PDF format)
Navident | NaviENT

EUROPE – Declarations of Conformity (PDF format)
Navident | MicronTracker | NaviENT

UNITED STATES – FDA 510(k) cleared devices 
Navident

SINGAPORE – Devices listed in Singapore Medical Device Register
Navident 

GLOBAL REGULATORY REPRESENTATIVES

Shown below are in-country regulatory representatives for issues and incident reporting. 

AUSTRALIA – Sponsor Representative
Emergo Australia, Sydney, Australia
Telephone: +61.2.9006.1662

EUROPE – Authorized Representative
Emergo Europe, The Hague, Netherlands
Telephone: +31.70.345.8570

SINGAPORE – Registrant
QST Dental PTE. LTD.
150 Kampong Ampat, KA Centre #07-01, Singapore 368324
Tel. No. : 93864634 Fax No. : 62736260

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