Documentation pain management and physical medicine practices typically request
Outpatient pain management and physical medicine groups generally route a new vendor request through the physician owner or a practice administrator before a product is added to inventory. That review usually starts with the certificate of analysis for the specific lot, a donor eligibility summary, and the lot release record showing quarantine and sterility testing were completed. Registration and licensure documentation for the supplying entity is also commonly requested and can be provided on request to verified accounts.
Sacramento
NPPES registry listings, primary taxonomy, retrieved 2026-10-27
206- Pain Medicine
- 74
- Physical Medicine & Rehabilitation
- 132
Confirming regulatory posture with the California medical board
Because Wharton's jelly and exosome products sit in different regulatory categories, we recommend a practice confirm its intended use and purchasing decisions directly with the California medical board and its own legal counsel before adding either product family to its formulary. Precision Biologics does not advise on clinical use, dosing, or procedures, and nothing in our documentation should be read as a recommendation for a specific application.
Opening an NPI-verified account
Accounts are opened using the NPI number of a licensed physician or the clinic's organizational NPI, which is how we confirm an order originates from a licensed practice rather than a direct consumer. Once verified, a practice can request supplier-level literature and characterization data for the exosome products in the catalog, along with the Wharton's jelly product documentation, ahead of any purchase.
Receiving shipments in the Sacramento area
Cryopreserved Wharton's jelly products are shipped overnight on dry ice in validated containers and should move into ultra-low temperature storage at -80 degrees C immediately on arrival. Lyophilized formats do not require cryogenic storage, which can simplify receiving for practices with multiple treatment rooms or satellite locations in the Sacramento area. Lot numbers travel with each shipment so the receiving clinic can track product by lot down to the patient record.
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
Does Precision Biologics have a representative based in Sacramento?+
No. Accounts are managed remotely through NPI verification and documentation review, and support is available to any verified account regardless of location.
What's required to open an account as a pain management practice?+
A valid NPI number tied to a licensed physician or practice, confirmation that the account is for a licensed clinic, and agreement to the terms covering documentation and ordering. Pricing is available to verified accounts only.
How is product traceability maintained once a shipment reaches our clinic?+
Each lot carries a unique identifier assigned during processing. Clinics are expected to log that identifier at the patient record level so a specific lot can be traced after use.