Contract manufacturerResolution Medical (Minneapolis, MN)MinnesotaCardiovascularEar, nose and throatNeurologyGastroenterology and urologyHematologyClass II
Resolution Medical
Contract manufacturer ยท Minneapolis, MN
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3012266672 (openFDA record; or search FDA's registration database)
- FEI number
- 3012266672
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- Resolution Medical, LLC (FDA owner/operator no. 10050670)
- Registered address
- 42 Northern Stacks Drive, Suite 200, Minneapolis, MN 55421
- Contract listings
- 8 device listings, 7 product codes, first listed Dec 14, 2015
- 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 |
|---|---|---|---|---|---|
| DQY | Catheter, Percutaneous | Class II | Cardiovascular | Contract manufacturing | Dec 21, 2022 |
| ETD | Tube, Tympanostomy | Class II | Ear, nose and throat | Contract manufacturing | Aug 5, 2022 |
| GWM | Device, Monitoring, Intracranial Pressure | Class II | Neurology | Contract manufacturing | Jan 17, 2024 |
| GZF | Stimulator, Peripheral Nerve, Implanted (Pain Relief) | Class II | Neurology | Contract manufacturing | Dec 14, 2015 |
| KLA | Monitor, Esophageal Motility, Anorectal Motility, And Tube | Class II | Gastroenterology and urology | Contract manufacturing | Dec 27, 2019 |
| KTI | Bronchoscope Accessory | Class II | Ear, nose and throat | Contract manufacturing | Mar 22, 2023 |
| ORG | Platelet And Plasma Separator For Bone Graft Handling | Class II | Hematology | Contract manufacturing | Jan 19, 2024 |