B2B Partnership Program
Add Advanced
Regenerative Protocols to Your Practice.
We're selective about who we partner with. That's what makes it valuable. PureExos partners get access to the full ecosystem — devices, consultation-gated biologics, training, and distribution support across Chicago and Cabo San Lucas.
Chicago & Cabo San Lucas operations
Authorized US & Mexico LIMFA® distributor
Full clinical training & onboarding
Expanding partner network
LIMFA® — Authorized Access
PureExos is an authorized US & Mexico distributor for LIMFA®. Offer your patients the same bio-electromagnetic technology used in the recovery rooms of elite European clubs, per the manufacturer — FDA 510(k) cleared (K243165), made in Italy by Eywa srl.
Red Light — Photobiomodulation
FDA Class II red-light therapy beds. Dual 660/850nm wavelengths, up to 196 J/cm² delivered dose, and up to 3,200 medical-grade LEDs — full-body sessions in 8–15 minutes. US-made, with clinical training and marketing assets included.
Biologics — Clinical-Team Access
MSC Exosomes and Therapeutic Peptides accessed through our clinical team. cGMP-manufactured exosomes — 100 billion signaling vesicles per vial, with batch traceability and a Certificate of Analysis. Consultation-gated and physician-directed for appropriate patients.
Who this is for
Serious clinics only.
- Pain management clinics
- Medical spas & wellness centers
- Chiropractic & recovery centers
- Sports medicine practices
- Functional medicine providers
- Multi-location operators
What partners get
The full ecosystem.
- Authorized LIMFA® access — US & Mexico
- Full product line: devices & biologics
- Biologics clinical-team access for your patients
- Marketing & social media assets
- Clinical training & onboarding
- Partner program for referrals
- Chicago & Cabo San Lucas distribution support
The process
Simple and fast.
Submit your application. Leo reviews it personally within 48 hours. If it's a fit, we schedule a 20-minute call — no pressure, no pitch. Just a real conversation about whether this makes sense for your practice.
PureExos distributes regenerative wellness devices and consultation-gated biologic options in the US and Mexico. Devices are described according to their individual regulatory status: LIMFA® is an FDA-cleared Class II device (510(k) K243165); Red Light therapy beds are FDA Class II devices; the Centropix KLOUD is an FDA-registered Class 1 device. Biologic options — including MSC exosomes and peptides — are provided for educational information only, are not FDA-approved, and when required are accessed following a consultation and approval by our clinical team or a licensed physician. Nothing on this page is intended to diagnose, treat, cure, or prevent any disease. Individual experiences vary.
