Contract manufacturerACCUMOLD LLC (Ankeny, IA)IowaNeurologyClass III
ACCUMOLD LLC
Contract manufacturer ยท Ankeny, IA
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3009627506 (openFDA record; or search FDA's registration database)
- FEI number
- 3009627506
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- AccuMold LLC (FDA owner/operator no. 10095628)
- Registered address
- 1711 Se Oralabor Rd, Ankeny, IA 50021
- Contract listings
- 1 device listings, 1 product codes, first listed Apr 6, 2026
- 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 |
|---|
| PMP | Dorsal Root Ganglion Stimulator For Pain Relief | Class III | Neurology | Contract manufacturing | Apr 6, 2026 |