Contract manufacturerIntriCon Corporation VH (Vadnais Heights, MN)MinnesotaGeneral hospitalClinical chemistryClass IIClass III
IntriCon Corporation VH
Contract manufacturer ยท Vadnais Heights, MN
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3007939342 (openFDA record; or search FDA's registration database)
- FEI number
- 3007939342
- Registered for
- FDA registration year 2027
- Establishment types
- Contract manufacturer
- Owner or operator
- INTRICON CORPORATION (FDA owner/operator no. 9039676)
- Registered address
- 4400 McMenemy St, Vadnais Heights, MN 55127
- Contract listings
- 10 device listings, 7 product codes, first listed Jan 11, 2013
- 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 |
|---|---|---|---|---|---|
| FMI | Needle, Hypodermic, Single Lumen | Class II | General hospital | Contract manufacturing | Jan 11, 2013 |
| FPA | Set, Administration, Intravascular | Class II | General hospital | Contract manufacturing | Jan 11, 2013 |
| FRN | Pump, Infusion | Class II | General hospital | Contract manufacturing | Dec 10, 2015 |
| LJT | Port & Catheter, Implanted, Subcutaneous, Intravascular | Class II | General hospital | Contract manufacturing | Jan 11, 2013 |
| LZG | Pump, Infusion, Insulin | Class II | General hospital | Contract manufacturing | Dec 10, 2015 |
| MDS | Sensor, Glucose, Invasive | Class III | Clinical chemistry | Contract manufacturing | Dec 20, 2013 |
| OZO | Automated Insulin Dosing , Threshold Suspend | Class III | Clinical chemistry | Contract manufacturing | Dec 20, 2013 |