Topeka
NPPES registry listings, primary taxonomy, retrieved 2026-10-27
15- Dermatology
- 10
- Plastic Surgery
- 5
NPI verification for medspa accounts
Because many medspas and aesthetic practices operate under a supervising physician rather than a separate facility NPI, Precision Biologics verifies the NPI of the physician or medical director tied to the practice during account setup.
This keeps ordering authority with a licensed individual and gives the practice a record it can point to if a payer, regulator, or internal compliance review ever asks about its vendor relationships.
Receiving cold-chain shipments
Cryopreserved Wharton's jelly and exosome products arrive overnight on dry ice in a validated shipping container and should move into -80 degree C storage promptly on receipt. Lyophilized formats are shelf-stable and are handled according to the insert included with the lot, which can be simpler for a practice without freezer capacity.
We recommend deciding in advance who signs for deliveries and where lot numbers get recorded before the first shipment arrives.
Documentation to request before stocking a product
Verified accounts can request the certificate of analysis, donor eligibility summary, and lot release record for a specific lot, along with the supplier's processing description, before a product is added to inventory.
For exosome products, characterization data reported by the supplier, including particle concentration and marker testing, is available on request so a medical director can review the record directly.
- Certificate of analysis
- Donor eligibility summary
- Lot release record
- Supplier processing description
Confirming regulatory fit
Precision Biologics does not advise on treatment protocols or which product suits a specific aesthetic use; that decision belongs to the supervising physician and the practice's legal counsel.
We recommend confirming any open regulatory question with the Kansas medical board. Verified accounts can schedule a physician-level conversation about product documentation through their account representative.
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 our medspa need its own NPI, or can we use our medical director's?+
Accounts are tied to the NPI of a licensed physician or medical director associated with the practice, which is the typical setup for medspas operating under physician supervision.
What cold-chain requirements should we plan for before our first order?+
Cryopreserved products require prompt transfer to -80 degree C storage on arrival; lyophilized products are shelf-stable and handled per the included insert. Confirm exact handling with your account representative.
How do we verify documentation before stocking a new product?+
Request the certificate of analysis, donor eligibility summary, and lot release record for the specific lot, along with the processing description, through your verified account.