Davenport
NPPES registry listings, primary taxonomy, retrieved 2026-10-27
9- Dermatology
- 5
- Plastic Surgery
- 4
Documentation to request before adding a supplier
Medspas and dermatology or aesthetic surgery practices considering a new biologics supplier typically start by requesting the certificate of analysis, donor eligibility summary, and lot release record for the specific lot under consideration, along with a copy of the supplier's registration and licensure documentation. Precision Biologics makes this documentation available to verified accounts rather than publishing it generally.
- Certificate of analysis for the lot
- Donor eligibility summary
- Lot release record
- Registration and licensure documentation for the supplier
Physician oversight and state verification
Because Precision Biologics sells only to licensed clinics, medspas operating under physician supervision, and physicians, the medical director of record is the person who typically signs off on a new product line and confirms it fits the practice's regulatory posture. That review should include your own counsel's read of how a specific intended use maps to the applicable federal framework.
We recommend confirming your practice's standing with the Iowa medical board as part of that internal process; Precision Biologics does not perform that verification on a practice's behalf.
Setting up an NPI-verified account
Account setup starts with an NPI number connected to the licensed clinic or physician associated with the medspa or practice. Once that account is verified, your team can request specifications and pricing for the Wharton's jelly and exosome product families, which are available to verified accounts only.
Shipping and cold-chain handling for the Midwest
Cryopreserved formats ship overnight on dry ice in validated containers from -80 degree C storage, and should be received and logged the day they are scheduled to arrive. Lyophilized formats are shelf-stable and ship without the same cold-chain requirement, arriving with a product insert specific to that lot.
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 medspa order directly, or does it need a supervising physician on the account?+
Accounts are opened under a licensed clinic or physician. A medspa operating under physician supervision can be verified through that physician's NPI as part of our standard account process.
What documentation comes with each shipment?+
Lot-specific documentation such as the certificate of analysis, donor eligibility summary, and lot release record is available to verified accounts for the lot they are purchasing.
Is pricing published for Davenport-area accounts?+
No. Pricing is available to verified accounts only, regardless of location, once NPI and license verification is complete.