Very quickly. New distributors can start selling immediately after a short hands-on training session. If your market requires local regulatory registration, we provide all the documentation and support needed to fast-track approval, so you can be in front of customers as soon as possible.

Availability changes as our network grows. Some markets have an exclusive partner, others are open to additional distributors. Send us your target country and we will tell you whether the territory is open, shared, or fully exclusive, and what the realistic path forward looks like.

Yes, in qualifying territories. Exclusivity is offered to partners who can demonstrate clinical reach in the target market, service capability, and a credible commercial plan that supports a sustained sales pipeline. Exclusivity is reviewed annually against agreed performance criteria.

Viasonix maintains FDA 510(k) clearance and CE MDR certification across the Falcon and Dolphin product lines, plus ISO 13485 quality-system certification at the company level. We supply distributors with the certificates, declarations of conformity, technical files, and labeling documentation needed for registration with local authorities such as TGA, ANVISA, NMPA, KFDA, TFDA, INVIMA, HSA, and others.

Training covers everything you need to get started: clinical applications, basic operation, unique features, installation, and basic service. By the end of training your team is ready to demo, sell, and support Viasonix systems with confidence.