Contract manufacturerCIRTEC MEDICAL (Brooklyn Park, MN)MinnesotaNeurologyOrthopedicPhysical medicineClass IIIClass II
CIRTEC MEDICAL
Contract manufacturer ยท Brooklyn Park, MN
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3013368220 (openFDA record; or search FDA's registration database)
- FEI number
- 3013368220
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- Cirtec Medical Corporation (FDA owner/operator no. 10025422)
- Registered address
- 9200 Xylon Avenue North, Brooklyn Park, MN 55445
- Contract listings
- 3 device listings, 3 product codes, first listed Sep 7, 2021
- 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 |
|---|---|---|---|---|---|
| LGW | Stimulator, Spinal-Cord, Totally Implanted For Pain Relief | Class III | Neurology | Contract manufacturing | Nov 1, 2024 |
| QPP | Implantable Post-Surgical Kinematic Measurement Knee Device | Class II | Orthopedic | Contract manufacturing | Sep 7, 2021 |
| QPY | Stimulator, Autonomic Nerve, Implanted For Stroke Rehabilitation | Class III | Physical medicine | Contract manufacturing | Nov 4, 2022 |