Contract manufacturerINTRICON CORPORATION (Arden Hills, MN)MinnesotaRadiologyClinical chemistryClass IIClass III
INTRICON CORPORATION
Contract manufacturer ยท Arden Hills, MN
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 2134850 (openFDA record; or search FDA's registration database)
- FEI number
- 3003007876
- Registered for
- FDA registration year 2026
- Establishment types
- Manufacturer; Contract manufacturer
- Owner or operator
- INTRICON CORPORATION (FDA owner/operator no. 9039676)
- Registered address
- 1260 Red Fox Rd, Arden Hills, MN 55112
- Contract listings
- 7 device listings, 4 product codes, first listed Jan 23, 2017
- 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 |
|---|---|---|---|---|---|
| JAK | System, X-Ray, Tomography, Computed | Class II | Radiology | Contract manufacturing | Feb 10, 2023 |
| MDS | Sensor, Glucose, Invasive | Class III | Clinical chemistry | Contract manufacturing | Jan 23, 2017 |
| OZO | Automated Insulin Dosing , Threshold Suspend | Class III | Clinical chemistry | Contract manufacturing | Jan 23, 2017 |
| OZP | Automated Insulin Dosing Device System, Single Hormonal Control | Class III | Clinical chemistry | Contract manufacturing | Nov 22, 2019 |