Port St. Lucie
NPPES registry listings, primary taxonomy, retrieved 2026-10-27
5- Dermatology
- 4
- Plastic Surgery
- 1
Receiving shipments at a Port St. Lucie medspa or dermatology practice
Cryopreserved Wharton's jelly formats ship overnight on dry ice in validated containers and need freezer capacity and a documented receiving step on arrival. Lyophilized exosome and Wharton's jelly formats are shelf-stable under normal storage, which some smaller aesthetic practices find easier to manage.
Every shipment is tracked by a unique lot identifier, so a practice can record exactly which lot was received and used at the patient-record level.
Documentation and Florida-specific verification
Before adding a new product, we recommend a Port St. Lucie medspa or dermatology practice request a certificate of analysis, donor eligibility summary, and sterility testing results for the specific lot, and confirm registration and licensure documentation can be produced on request.
Florida's SB 1768, effective July 1, 2025, permits certain MD/DO physicians to use non-FDA-approved stem cell therapies under specific conditions; it applies to physician use decisions under state law and does not change the federal FDA status of any product. A practice should verify applicability with the Florida Board of Medicine and its own counsel, not with Precision Biologics.
Opening an NPI-verified account
Because sales are limited to licensed clinics, physicians, and physician-supervised medspas, a Port St. Lucie account is opened under an NPI number tied to the supervising physician. A short verification step confirms the NPI and delivery address before pricing and ordering access are unlocked.
Account setup and support
Once verified, a practice can request a documentation packet for the specific products it is evaluating and schedule a peer-to-peer call on specifications and paperwork. Precision Biologics does not advise on procedures, dosing, or expected results; those determinations stay with the supervising physician and the practice's own counsel.
FDA has stated there are no FDA-approved exosome products. Exosome products are generally regulated as biologic drugs under section 351 of the Public Health Service Act, not as 361 HCT/Ps. Purchase and clinical use decisions belong to the physician with their own regulatory counsel.
These products are not FDA approved or licensed for any disease or condition. Information is for licensed healthcare professionals and is not medical or legal advice.
Frequently asked questions
Can a Port St. Lucie dermatology practice order without a supervising physician?+
No. Accounts are tied to an NPI number for a licensed physician, clinic, or physician-supervised medspa. We do not open accounts outside that structure.
Does Florida law change how these products are regulated federally?+
No. Florida's SB 1768 addresses physician use of certain non-FDA-approved stem cell therapies under state law; federal FDA regulation of any specific product is unchanged, and these products are not FDA approved.
What storage should a Port St. Lucie medspa plan for before ordering?+
That depends on the product format: cryopreserved formats need freezer space after overnight dry-ice delivery, while lyophilized formats are shelf-stable per the product insert supplied with the lot.