Products for Topical Aesthetic and Post-Procedure Workflows
Regulatory Notice: ExaVeyra Sciences is a B2B wholesale supplier. Product descriptions below are for procurement context only and are not therapeutic claims. Products are not intended to diagnose, treat, cure, or prevent any disease. All clinical and compliance decisions rest with the licensed practitioner.
Medspas and aesthetic clinics need topical biologic supply, device compatibility, and documentation that medical directors can review. ExaVeyra supports NPI-verified medspa accounts with biomolecular signaling vesicles, post-procedure serums, microneedling devices, and PRP/PRF kits.
Biomolecular signaling vesicles supplied in liquid format, cold-chain shipped, for topical aesthetic application by licensed practitioners.
Post-procedure serum procurement for medspas standardizing topical application workflows after microneedling protocols.
RF microneedling devices, standard microneedling pens, and PRP/PRF kits commonly paired with topical biologic protocols.
Chemist-guided supplier documentation review covering particle size distribution, surface markers, sterility, and lot records.
All biomolecular signaling vesicles ship cold-chain in temperature-monitored packaging. Liquid format only.
COA per lot, NTA particle count verification, and supporting supplier documentation available for approved accounts.
Important: ExaVeyra does not make clinical efficacy claims. Protocol design, patient selection, and clinical application are the responsibility of the licensed practitioner.
Supplier Documentation Reviewed Through an EV Lens
The MISEV 2023 framework gives medspa medical directors a way to evaluate extracellular vesicle documentation. ExaVeyra uses chemist-guided review of supplier records, including particle sizing, identity markers, sterility, endotoxin, and lot-specific testing.
Vesicle Documentation
- NTA particle count verification
- Particle size distribution
- Surface marker review
- Sterility testing
- Mycoplasma and endotoxin records
- COA per lot
Medspa Use Context
- Topical aesthetic application
- Post-procedure workflows
- Medical director review
- Cold-chain guidance
- Device compatibility support
- NPI-verified access
Approved accounts can request supplier documentation and stability information by lot so medical directors can evaluate fit for their practice protocols.
Recommended for Medspas and Aesthetic Clinics
All products require NPI verification and approved wholesale account. COA, lot documentation, and shipping guidance are available for approved practices.
Biomolecular Signaling Vesicles
MSC-derived, liquid format, cold-chain shipped, topical aesthetic use, MISEV 2023 framework.
Post-Procedure Serum
Topical post-microneedling application, bioactive formulation, cold-chain shipped.
RF Microneedling Device
Fractional RF, adjustable depth, compatible with topical biologic protocols.
PRP/PRF Kit
12 mL closed system, ideal for medspa hair and skin protocols.
What Medspa Teams Get From Our Supply Chain
NPI-Verified Access Only
Wholesale access is limited to licensed practitioners and practices with an active medical director or supervising physician NPI.
MISEV-Aligned Review
Our chemist-guided evaluation process reviews supplier records through the MISEV 2023 extracellular vesicle documentation framework.
COA Per Lot
Every biologic lot is supported by documentation covering particle count, sterility, mycoplasma, endotoxin, and supplier testing records.
Cold-Chain Support
Liquid biomolecular signaling vesicles ship with temperature-monitored cold-chain packaging and expedited fulfillment.
Device Compatibility
RF microneedling devices, microneedling pens, and PRP/PRF kits can be sourced alongside topical biologic supply.
Medical Director Documentation
Approved accounts can request documentation packages to support internal protocol review and procurement records.
Questions from Medspa and Aesthetic Clinic Teams
What exosome products does ExaVeyra supply for medspas?+
ExaVeyra supplies MSC-derived biomolecular signaling vesicles for topical aesthetic treatments. Available in liquid format, cold-chain shipped. All products are supplied under the MISEV 2023 framework with COA per lot, NTA particle count verification, and cold-chain shipping. For medspa use, products are labeled for topical aesthetic application only.
Are your exosomes FDA-approved?+
No exosome product currently holds FDA approval for therapeutic use in humans. ExaVeyra supplies biomolecular signaling vesicles for topical aesthetic treatments by licensed practitioners. All products are sourced from FDA-registered facilities with full COA documentation. Practitioners are responsible for compliance with applicable regulations.
What is the MISEV 2023 framework?+
MISEV 2023 is the Minimal Information for Studies of Extracellular Vesicles guidelines published by the International Society for Extracellular Vesicles. ExaVeyra uses this framework to evaluate supplier documentation including particle size distribution, surface marker verification, and sterility testing. Our chemist-guided COA evaluation guide covers all 12 MISEV-aligned parameters.
Do you supply devices compatible with topical exosome protocols?+
Yes. ExaVeyra supplies RF microneedling devices, standard microneedling pens, and PRP/PRF kits that are commonly used in conjunction with topical biologic protocols. Device compatibility documentation is available on request.
What are your shipping requirements for liquid exosomes?+
Liquid biomolecular signaling vesicles require cold-chain shipping. ExaVeyra uses temperature-monitored packaging with expedited fulfillment. Lyophilized formats ship ambient and have extended stability. Contact our team for stability data per lot.
Can medspas without a medical director apply for wholesale access?+
ExaVeyra supplies to NPI-verified licensed practitioners. A medical director or supervising physician with an active NPI is required for wholesale account approval. Our team can advise on the documentation required during the application process.