Contract manufacturerMOLDED PRODUCTS INC. (Harlan, IA)IowaGastroenterology and urologyClass IClass II
MOLDED PRODUCTS INC.
Contract manufacturer ยท Harlan, IA
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 1932668 (openFDA record; or search FDA's registration database)
- FEI number
- 1000138417
- Registered for
- FDA registration year 2026
- Establishment types
- Complaint file establishment; Manufacturer; Contract manufacturer; Repackager or relabeler
- Owner or operator
- MOLDED PRODUCTS INC. (FDA owner/operator no. 9007334)
- Registered address
- 1812 Industrial Pkwy, Harlan, IA 51537
- Contract listings
- 3 device listings, 3 product codes, first listed Nov 30, 1994
- 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 |
|---|---|---|---|---|---|
| FHA | Clamp, Penile | Class I | Gastroenterology and urology | Contract manufacturing | Nov 25, 2020 |
| GBM | Catheter, Urethral | Class II | Gastroenterology and urology | Contract manufacturing | Jan 10, 2022 |
| LIF | Dialyzer Reprocessing System | Class II | Gastroenterology and urology | Contract manufacturing | Nov 30, 1994 |