Contract manufacturer3DPX MEDICAL (Chicago, IL)IllinoisDentalClass IIUnclassified
3DPX MEDICAL
Contract manufacturer ยท Chicago, IL
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3017567754 (openFDA record; or search FDA's registration database)
- FEI number
- 3017567754
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- 3DPX Medical (FDA owner/operator no. 10078770)
- Registered address
- 410 N Milwaukee Ave Suite 100, Chicago, IL 60607
- Contract listings
- 2 device listings, 3 product codes, first listed Mar 11, 2021
- 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 |
|---|---|---|---|---|---|
| LRK | Device, Anti-Snoring | Class II | Dental | Contract manufacturing | Mar 11, 2021 |
| MQC | Mouthguard, Prescription | Unclassified | Dental | Contract manufacturing | Feb 27, 2025 |
| OCO | Mouthguard, Migraine/Tension Headache | Unclassified | Dental | Contract manufacturing | Feb 27, 2025 |