Contract manufacturerCARRIO CABLING CORPORATION (Colorado Springs, CO)ColoradoCardiovascularClass IIClass III
CARRIO CABLING CORPORATION
Contract manufacturer ยท Colorado Springs, CO
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3006634485 (openFDA record; or search FDA's registration database)
- FEI number
- 3006634485
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- CARRIO CABLING CORPORATION (FDA owner/operator no. 10045507)
- Registered address
- 4920 Centennial Blvd, Colorado Springs, CO 80919
- Contract listings
- 4 device listings, 4 product codes, first listed Oct 6, 2023
- 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 |
|---|---|---|---|---|---|
| DRF | Catheter, Electrode Recording, Or Probe, Electrode Recording | Class II | Cardiovascular | Contract manufacturing | Apr 17, 2024 |
| DSA | Cable, Transducer And Electrode, Patient, (Including Connector) | Class II | Cardiovascular | Contract manufacturing | Oct 6, 2023 |
| LPB | Cardiac Ablation Percutaneous Catheter | Class III | Cardiovascular | Contract manufacturing | Jul 8, 2024 |
| OAD | Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter | Class III | Cardiovascular | Contract manufacturing | Jul 8, 2024 |