Contract manufacturerMEDICAL MURRAY, INC. (Lake Zurich, IL)IllinoisGastroenterology and urologyCardiovascularGeneral hospitalClass IIClass III
MEDICAL MURRAY, INC.
Contract manufacturer ยท Lake Zurich, IL
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 1424778 (openFDA record; or search FDA's registration database)
- FEI number
- 3003473227
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- MURRAY, INC. (FDA owner/operator no. 9046685)
- Registered address
- 540 Capital Drive, Suite 150, Lake Zurich, IL 60047
- Contract listings
- 7 device listings, 8 product codes, first listed Nov 20, 2014
- 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 |
|---|---|---|---|---|---|
| FAD | Stent, Ureteral | Class II | Gastroenterology and urology | Contract manufacturing | Nov 1, 2024 |
| KRD | Device, Vascular, For Promoting Embolization | Class II | Cardiovascular | Contract manufacturing | Apr 10, 2018 |
| LJS | Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days | Class II | General hospital | Contract manufacturing | Mar 3, 2025 |
| MJN | Catheter, Intravascular Occluding, Temporary | Class II | Cardiovascular | Contract manufacturing | Nov 20, 2014 |
| NIM | Stent, Carotid | Class III | Cardiovascular | Contract manufacturing | Nov 12, 2024 |
| PNF | Aortic Stent | Class III | Cardiovascular | Contract manufacturing | Sep 4, 2024 |
| QEW | Peripheral Mechanical Thrombectomy With Aspiration | Class II | Cardiovascular | Contract manufacturing | Oct 25, 2023 |
| QWC | Pulmonary Stent | Class III | Cardiovascular | Contract manufacturing | Sep 4, 2024 |