Contract manufacturerPOLO CUSTOM PRODUCTS (Louisville, MS)MississippiCardiovascularGeneral hospitalClass IIClass I
POLO CUSTOM PRODUCTS
Contract manufacturer ยท Louisville, MS
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3016704581 (openFDA record; or search FDA's registration database)
- FEI number
- 3016704581
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- Polo Custom Products (FDA owner/operator no. 9919026)
- Registered address
- 15730 W Main Street, Louisville, MS 39339
- Contract listings
- 2 device listings, 2 product codes, first listed Dec 21, 2022
- Certification
- Not verified. We have no certification data for this facility yet.
Devices listed as contract work
Each row is an FDA product code this facility lists under its contract establishment type, with the date of its earliest such listing.
| Product code | Device (FDA name) | Class | Category | Role | First listed |
|---|---|---|---|---|---|
| DXC | Clamp, Vascular | Class II | Cardiovascular | Contract manufacturing | Dec 4, 2023 |
| PXD | Prep Kit | Class I | General hospital | Contract manufacturing | Dec 21, 2022 |