Only original SCENAR registered by FDA - RITM SCENAR

The internet highway is littered with information about SCENAR.  Whether you are a professional practitioner selecting a SCENAR for use in your practice or a consumer seeking one for home use please understand the importance of device registration in your country. 

The RITMSCENAR line is the only original SCENAR line FDA cleared in the U.S.   Protecting the public against products illegally marketed without FDA clearance is an important part of the mission of the FDA. 

Here at The SCENAR Experts, we have years of experience in the medical device industry - long before becoming distributors of the RITMSCENAR line of products.  We understand the importance of the medical device regulations. 

We receive calls inquiring about devices like the Cosmodic, asking us to compare it to the RITMSCENAR.  In the U.S. this is a conversation that should not be happening.  We tell all practitioners the Cosmodic is not registered in the U.S. and if they want to be compliant with their licensing body as well as insurance (if they are billing payers) they will not buy and use this device in their practice.  The technical and outcomes comparison conversation can't be had either as there is no data.

We are proud to share RITMSCENAR with practitioners and consumers in the United States.  It is the only FDA cleared original SCENAR.  The Pro Plus and Pro devices are FDA cleared for practitioners.  Only the Pro Plus is currently available in inventory.  The Pro inventory is gone - making way for the introduction of the new Super Pro once this exciting new model has its FDA clearance. 

The Sport D and Sport are cleared and available for consumers.  RITM OKB ZAO has developed the new Home Expert for home users.  This device is NOT FDA cleared for sales yet.  We will alert you when it is.  We are excited about its new features.

When it comes to seeking all the benefits of SCENAR partner with us, the U.S. experienced medical device industry professionals.