Contract manufacturerCLARITY DESIGN, INC. (Poway, CA)CaliforniaGeneral hospitalNeurologyCardiovascularGeneral and plastic surgeryClass II
CLARITY DESIGN, INC.
Contract manufacturer · Poway, CA
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3011883032 (openFDA record; or search FDA's registration database)
- FEI number
- 3011883032
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- Clarity Design Inc (FDA owner/operator no. 10049915)
- Registered address
- 13000 Gregg Street, Suite B, Poway, CA 92064
- Contract listings
- 6 device listings, 5 product codes, first listed Jan 3, 2018
- 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 |
|---|---|---|---|---|---|
| FRN | Pump, Infusion | Class II | General hospital | Contract manufacturing | Dec 26, 2025 |
| HCC | Device, Biofeedback | Class II | Neurology | Contract manufacturing | Sep 21, 2026 |
| MWJ | Electrocardiograph, Ambulatory (Without Analysis) | Class II | Cardiovascular | Contract manufacturing | Dec 31, 2025 |
| NEU | Marker, Radiographic, Implantable | Class II | General and plastic surgery | Contract manufacturing | Sep 21, 2026 |
| NFO | Stimulator, Transcutaneous Electrical, Aesthetic Purposes | Class II | Neurology | Contract manufacturing | Jan 3, 2018 |