Compliance
How we describe what we distribute — and the lines we hold to keep it accurate.
PureExos LLC distributes regenerative wellness devices and consult-gated biologic products. We take regulatory accuracy seriously and describe every product according to its actual regulatory status. This page summarizes how we present devices and biologics, and the safeguards built into how certain products are accessed.
Devices
Hardware we distribute is described according to its specific U.S. regulatory status. We do not apply a single blanket status across categories.
LIMFA
The LIMFA device holds U.S. FDA 510(k) clearance (K243165). Its cleared U.S. indication is to temporarily increase blood circulation in healthy leg muscles and to stimulate healthy muscles in order to improve and facilitate muscle performance. We do not represent the device beyond this cleared indication.
Red Light Wellness
Described according to its applicable FDA device classification.
KLOUD (PEMF)
Described according to its applicable FDA registration and classification.
Biologic products
Biologic products — including MSC exosomes, therapeutic peptides, and Wharton’s jelly — are presented for educational information only. They are not represented as FDA-approved. No exosome product is FDA-approved.
Biologic products are not offered for direct online purchase and are never sold through a shopping cart. They are available only following a consultation and, where required, evaluation and approval by our clinical team or a licensed physician.
How we describe products
- We describe each product according to its actual regulatory status — accurate per category, never a blanket claim.
- We do not make disease-treatment claims for devices or biologic products.
- We do not publish efficacy percentages in public-facing materials.
- Manufacturer and third-party relationships are described as manufacturer relationships, not as PureExos endorsements.
- Detailed clinical protocols and condition-specific information are reserved for qualified practitioners through gated materials.
Consultation safeguards
Consult-gated products are coordinated through our clinical team. Where required, exosome access follows evaluation and approval by a licensed physician. These steps are designed to ensure products are considered only where appropriate.
Reporting a concern
If you believe any statement on this Site is inaccurate or out of date, please tell us so we can review it promptly. Contact [email protected].
Contact us
PureExos LLC
1440 W Taylor St, #1113
Chicago, IL 60607
Email: [email protected]
Phone: [enable JavaScript to view]