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Wharton's Jelly

Instead of adding another separate ECM or filler step, providers get a single Wharton's Jelly-based human biologic that fits directly into current orthopedic, wound care, spine, sports medicine, and aesthetic services.

WHARTON'S JELLY
Umbilical Cord Wharton's Jelly (MXT-002)
  • Exosomes
  • 200+ Growth Factors
  • Biologically active cytokines
  • Natural human collagen
  • Natural human hyaluronic acid
  • Chondroitin sulfate
  • Full Lot & Donor Traceability
Wharton's Jelly vial — umbilical cord ECM with 200+ growth factors and natural collagen

How It Works

Mechanism of Action

Wharton's Jelly is the gelatinous connective tissue within the umbilical cord, naturally rich in collagen, hyaluronic acid, chondroitin sulfate, and Exosomes. Processed into MXT-002 using proprietary technique with no enzymes added, it retains this matrix as a ready-to-use, human-derived biologic.

For providers, that means Wharton's Jelly works in synergy with procedures already on the menu, used alone, or layered into orthopedic, wound care, spine, sports medicine, and aesthetic protocols to soothe and enhance the results patients already expect. Because MXT-002 arrives pre-processed and ready to administer, it adds to a service menu without the onsite processing or added chair time that comes with harvesting a patient's own tissue, making it as much a replacement for labor-intensive protocols as it is an enhancement to existing ones.

Testing & Safety

Facility
FDA Registered (FEI# 3017371366), Also inspected by Florida Dept. of Business & Professional Regulation, Division of Drugs, Devices & Cosmetics
Manufacturing Standard
Current Good Manufacturing Practice (cGMP)
Testing
Fully tested by an independent, third-party, CLIA-certified laboratory
Exosome Identity Testing
Tested for expression of Tetraspanins (CD9, CD86, CD81) — markers used to confirm exosome identity
Donor Eligibility
All birth tissue donors screened for eligibility per AATB and FDA standards
Source Tissue
Human Umbilical Cord Wharton's Jelly (MXT-002), collected by US recovery agencies
Processing
Proprietary processing techniques adhering to AATB and FDA standards; no enzymes used
Active Components
Collagen, Hyaluronic Acid, Chondroitin Sulfate, Exosomes, Growth Factors, Cytokines
Traceability
Full lot/donor per vial

Clinical Applications

Orthopedic

Joint, tendon, and cartilage support through ECM scaffolding and growth factor delivery for connective tissue repair and inflammation modulation.

Wound Healing

Chronic and acute wound management leveraging natural hyaluronic acid and collagen matrix to support tissue regeneration and healing.

Spine

Disc and spinal tissue support applications utilizing the cushioning and structural properties of Wharton’s Jelly matrix.

Sports Medicine

Athletic injury recovery and performance restoration through targeted growth factor delivery to damaged musculoskeletal tissues.

Aesthetics

Skin rejuvenation and facial restoration protocols leveraging the natural hyaluronic acid and collagen content for volume and hydration support.

Dental

Oral surgery recovery, bone grafting support, and periodontal tissue regeneration through ECM-based scaffolding and growth factor signaling.

Donor Infectious Disease Screening (11-Panel)

01

CMV Total Antibody

02

HBV Core Antibody (Hepatitis B Virus)

03

Hepatitis B Surface Antigen

04

Syphilis Screening (Non-treponemal)

05

HBV NAT/PCR

06

HTLV (Types I and II)

07

HCV Encoded Antigens (Hepatitis C Virus)

08

WNV (West Nile Virus)

09

HCV NAT/PCR

10

HIV (Types 1 & 2, plus O)

11

HIV-1/2 NAT/PCR

All testing is performed according to CDC, FDA, and US Organ Procurement and Transplantation Network policies. Donors are rejected for any reactive, positive, or equivocal result and accepted only when results are nonreactive, negative, or non-equivocal.

Compliance & Regulatory

FDA Registered (FEI# 3017371366) — laboratory partner
Florida DBPR, Division of Drugs, Devices & Cosmetics — facility inspected
cGMP
Third-Party CLIA-Certified Lab Testing
Full Lot & Donor Traceability
All products are processed and distributed by independently owned and operated FDA-registered laboratory partners. Sōlix does not manufacture, compound, or take possession of any biological product. Products are minimally manipulated human cells, tissues, and cellular and tissue-based products (HCT/Ps) regulated under 21 CFR Part 1271, intended for homologous use only. Administration is at the sole discretion of a licensed healthcare provider. The statements on this page have not been evaluated by the FDA. These products are not intended to diagnose, treat, cure, or prevent any disease.
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DISCLAIMER

Sōlix does not own, operate, or manage any laboratory, manufacturing, or compounding facility. All biological products available through this platform are manufactured, processed, and distributed by our independently owned and operated FDA-registered laboratory partners. Sōlix does not distribute, ship, handle, or take possession of any biological product at any point in the supply chain.

Sōlix operates as a provider platform that offers licensed healthcare practitioners access to product ordering, clinical education, implementation support, marketing resources, and business integration tools designed to help practices incorporate regenerative biologics into their clinical offerings.

Sōlix is not a compounding pharmacy or chemical compounding facility as defined under Section 503A or 503B of the Federal Food, Drug, and Cosmetic Act. Sōlix does not compound, manufacture, repackage, or relabel any drug or biological product.

Sōlix resources are for educational and informational purposes only. Providers are responsible for their own regulatory compliance, licensing, and insurance. Sōlix assumes no liability for how materials are applied in practice.

FDA DISCLAIMER

The statements made on this website have not been evaluated by the U.S. Food and Drug Administration. The products and services referenced on this platform are not intended to diagnose, treat, cure, or prevent any disease or medical condition. Biological products, including but not limited to stem cells, exosomes, Wharton's Jelly, and amniotic tissue allografts, are minimally manipulated human cells, tissues, and cellular and tissue-based products (HCT/Ps) regulated under 21 CFR Part 1271. These products are intended for homologous use only and are administered at the sole discretion of a licensed healthcare provider following individual patient assessment. Results may vary. No guarantees of specific outcomes are made or implied.

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