Contract manufacturerImpilo Phoenix (Phoenix, AZ)ArizonaCardiovascularClinical chemistryClass II
Impilo Phoenix
Contract manufacturer · Phoenix, AZ
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3031789039 (openFDA record; or search FDA's registration database)
- FEI number
- 3031789039
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer; Repackager or relabeler
- Owner or operator
- Impilo Health (FDA owner/operator no. 10086162)
- Registered address
- 2675 W Buckeye Rd, Suite 200 Phoenix, Phoenix, AZ 85009
- Contract listings
- 3 device listings, 3 product codes, first listed Jul 3, 2025
- 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 |
|---|---|---|---|---|---|
| DXN | System, Measurement, Blood-Pressure, Non-Invasive | Class II | Cardiovascular | Contract manufacturing | Mar 20, 2026 |
| NBW | System, Test, Blood Glucose, Over The Counter | Class II | Clinical chemistry | Contract manufacturing | Mar 20, 2026 |
| PQD | Blood Specimen Collection Convenience Kit (Excludes Hiv) | Class II | Clinical chemistry | Contract manufacturing | Jul 3, 2025 |