Contract manufacturerRose Medical (Grand Rapids, MI)MichiganCardiovascularGastroenterology and urologyNeurologyClass IIClass I
Rose Medical
Contract manufacturer ยท Grand Rapids, MI
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 1836324 (openFDA record; or search FDA's registration database)
- FEI number
- 3002998595
- Registered for
- FDA registration year 2027
- Establishment types
- Contract manufacturer
- Owner or operator
- Rose Medical (FDA owner/operator no. 10042209)
- Registered address
- 1440 Front Ave NW, Grand Rapids, MI 49504
- Contract listings
- 6 device listings, 7 product codes, first listed Nov 1, 2012
- 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 |
|---|---|---|---|---|---|
| DWF | Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass | Class II | Cardiovascular | Contract manufacturing | Jun 7, 2019 |
| FED | Endoscopic Access Overtube, Gastroenterology-Urology | Class II | Gastroenterology and urology | Contract manufacturing | Nov 1, 2012 |
| FFX | System, Gastrointestinal Motility (Electrical) | Class II | Gastroenterology and urology | Contract manufacturing | Apr 7, 2025 |
| GWM | Device, Monitoring, Intracranial Pressure | Class II | Neurology | Contract manufacturing | Oct 31, 2016 |
| JXG | Shunt, Central Nervous System And Components | Class II | Neurology | Contract manufacturing | Jun 7, 2023 |
| KLA | Monitor, Esophageal Motility, Anorectal Motility, And Tube | Class II | Gastroenterology and urology | Contract manufacturing | Apr 7, 2025 |
| MWS | Stabilizer, Heart | Class I | Cardiovascular | Contract manufacturing | Jun 7, 2023 |