Contract manufacturerKimball Solutions - Indianapolis (Indianapolis, IN)IndianaGeneral and plastic surgeryOrthopedicClass II
Kimball Solutions - Indianapolis
Contract manufacturer ยท Indianapolis, IN
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3047841690 (openFDA record; or search FDA's registration database)
- FEI number
- 3047841690
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- KIMBALL SOLUTIONS GROUP, LLC (FDA owner/operator no. 9071700)
- Registered address
- 1220 S Post Rd, Indianapolis, IN 46239
- Contract listings
- 3 device listings, 4 product codes, first listed Dec 20, 2024
- 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 |
|---|---|---|---|---|---|
| GEI | Electrosurgical, Cutting & Coagulation & Accessories | Class II | General and plastic surgery | Contract manufacturing | Dec 9, 2025 |
| HRX | Arthroscope | Class II | Orthopedic | Contract manufacturing | Dec 20, 2024 |
| JCX | Apparatus, Suction, Ward Use, Portable, Ac-Powered | Class II | General and plastic surgery | Contract manufacturing | Mar 26, 2026 |
| SFQ | Electrosurgical, Cutting & Coagulation & Accessories, For Cardiac Electrophysiology Device Implantation And Revision | Class II | General and plastic surgery | Contract manufacturing | Dec 9, 2025 |