Contract manufacturerGreatbatch Medical (Minneapolis, MN)MinnesotaCardiovascularAnesthesiologyClass IIIClass II
Greatbatch Medical
Contract manufacturer · Minneapolis, MN
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 2183787 (openFDA record; or search FDA's registration database)
- FEI number
- 2183787
- Registered for
- FDA registration year 2026
- Establishment types
- Complaint file establishment; Specification developer; Manufacturer; Contract manufacturer
- Owner or operator
- GREATBATCH MEDICAL (FDA owner/operator no. 9035261)
- Registered address
- 2300 Berkshire Lane North, Minneapolis, MN 55441
- Contract listings
- 3 device listings, 4 product codes, first listed Dec 10, 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 |
|---|---|---|---|---|---|
| LWS | Implantable Cardioverter Defibrillator (Non-Crt) | Class III | Cardiovascular | Contract manufacturing | Dec 10, 2014 |
| MNQ | Stimulator, Hypoglossal Nerve, Implanted, Apnea | Class III | Anesthesiology | Contract manufacturing | Dec 10, 2014 |
| MTD | Catheter, Intracardiac Mapping, High-Density Array | Class II | Cardiovascular | Contract manufacturing | Feb 11, 2025 |
| NVY | Permanent Defibrillator Electrodes | Class III | Cardiovascular | Contract manufacturing | Dec 10, 2014 |