Contract manufacturerGMI CORPORATION (Franklin, IN)IndianaNeurologyGeneral and plastic surgeryGastroenterology and urologyUnclassifiedClass IClass II
GMI CORPORATION
Contract manufacturer · Franklin, IN
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3011743372 (openFDA record; or search FDA's registration database)
- FEI number
- 3011743372
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- GMI Corporation (FDA owner/operator no. 10052677)
- Registered address
- 700 International Dr, Franklin, IN 46131
- Contract listings
- 6 device listings, 6 product codes, first listed Sep 9, 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 |
|---|---|---|---|---|---|
| BWK | Stimulator, Electro-Acupuncture | Unclassified | Neurology | Contract manufacturing | Nov 10, 2020 |
| GCY | Apparatus, Suction, Single Patient Use, Portable, Nonpowered | Class I | General and plastic surgery | Contract manufacturing | Nov 11, 2021 |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories | Class II | General and plastic surgery | Contract manufacturing | Sep 9, 2016 |
| GZT | Retractor, Self-Retaining, For Neurosurgery | Class II | Neurology | Contract manufacturing | Nov 9, 2017 |
| PZR | Percutaneous Nerve Stimulator For Opioid Withdrawal | Class II | Neurology | Contract manufacturing | Feb 5, 2021 |
| QHH | Non-Implanted Nerve Stimulator For Pain Associated With Irritable Bowel Syndrome (Ibs) | Class II | Gastroenterology and urology | Contract manufacturing | Nov 10, 2020 |