Dayton
NPPES registry listings, primary taxonomy, retrieved 2026-10-27
94- Orthopaedic Surgery
- 94
Vendor qualification for orthopedic groups
Orthopedic practices and ambulatory surgery centers generally qualify a tissue or biologics supplier before any purchasing decision, reviewing processing documentation, donor eligibility screening, and lot release records rather than taking marketing claims at face value.
Precision Biologics supports this review by making a certificate of analysis, a donor eligibility summary, and a lot release record available for each lot on request to verified accounts.
NPI-verified accounts and ordering
Every account is verified against an NPI number before an order can be placed, consistent with the way practices already track prescribing and billing credentials internally.
Pricing is not published and is shared only with verified accounts once an order inquiry is underway.
Receiving cryopreserved shipments in the Midwest
Cryopreserved Wharton's jelly and exosome products are frozen using a slow-rate process, stored at -80 degrees Celsius, and shipped overnight on dry ice in validated containers to clinics across the Midwest region.
A practice receiving a shipment should confirm the shipment arrived intact, log the lot number against the shipment record, and move product directly into -80 degree Celsius storage before use, maintaining the lot-level traceability a clinic will later tie to its own patient records.
- Confirm dry ice and container integrity on arrival
- Record the lot number from the shipment label
- Transfer product to -80 C storage without delay
- File the lot documentation with the order record
Documentation review and account setup
Because Dayton practices operate under Ohio licensure and their own clinical and legal judgment, we recommend verifying any planned use of these products with the practice's medical director, its own counsel, and the Ohio medical board rather than relying on supplier materials alone.
Our team supports account setup with NPI verification, documentation requests, and access to physician-level calls focused on product documentation; these conversations do not constitute clinical or legal advice.
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 sell directly to solo orthopedic practices in Dayton, or only to larger groups?+
Accounts are open to any licensed physician practice or physician-supervised clinic that completes NPI verification, regardless of the number of locations.
What documentation should a Dayton orthopedic practice request before its first order?+
Ask for the certificate of analysis, the donor eligibility summary, and the lot release record for the specific lot being quoted, and route them to your medical director and counsel for review.
How is product traceability maintained after a shipment arrives at an Ohio clinic?+
Each lot carries a unique identifier assigned at processing; clinics are expected to log that identifier against patient records on their side so use can be traced back to the specific lot.