Contract manufacturerCDR Manufacturing, Inc., DBA Keytronic (Oakdale, MN)MinnesotaCardiovascularRadiologyAnesthesiologyClass IIClass III
CDR Manufacturing, Inc., DBA Keytronic
Contract manufacturer · Oakdale, MN
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3003857828 (openFDA record; or search FDA's registration database)
- FEI number
- 3003857828
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- Key Tronic (FDA owner/operator no. 10050703)
- Registered address
- 7015 55TH ST N, Oakdale, MN 55128
- Contract listings
- 7 device listings, 8 product codes, first listed Dec 15, 2016
- 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 |
|---|---|---|---|---|---|
| DPS | Electrocardiograph | Class II | Cardiovascular | Contract manufacturing | Dec 15, 2016 |
| DSB | Plethysmograph, Impedance | Class II | Cardiovascular | Contract manufacturing | Jun 19, 2018 |
| DWJ | System, Thermal Regulating | Class II | Cardiovascular | Contract manufacturing | Jan 27, 2017 |
| IYO | System, Imaging, Pulsed Echo, Ultrasonic | Class II | Radiology | Contract manufacturing | Jan 22, 2021 |
| LOS | Product code LOS (not in FDA's classification file) | – | – | Contract manufacturing | Dec 15, 2016 |
| MLD | Monitor, St Segment With Alarm | Class II | Cardiovascular | Contract manufacturing | Dec 15, 2016 |
| MNQ | Stimulator, Hypoglossal Nerve, Implanted, Apnea | Class III | Anesthesiology | Contract manufacturing | Feb 16, 2022 |
| OBH | Monitor, Extracellular Fluid, Lymphedema, Extremity | Class II | Cardiovascular | Contract manufacturing | Jun 19, 2018 |