FDA Registration
Active
🇺🇸 United States
CLARITY DESIGN, INC.
Reg #: 3011883032
·
FEI: 3011883032
·
Expires 2026
Products
3
Proprietary Names
2
Establishment Types
1
Classifications
3
Registration Details
- Registration Name
- CLARITY DESIGN, INC.
- Registration Number
- 3011883032
- FEI Number
- 3011883032
- Status
- Active
- Expiry Year
- 2026
- Initial Importer
- No
- Address
- 13000 Gregg Street, Suite B
- City
- Poway
- State
- CA
- ZIP
- 92064
- Country
- US
Owner / Operator
- Firm Name
- Clarity Design Inc
- Operator Number
- 10049915
- Address
- 13000 Gregg Street, Suite B
- City
- Poway
- State
- CA
- Postal Code
- 92064
- Country
- US
- Correspondent
- Thomas H Lupfer
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Stimulator, Transcutaneous Electrical, Aesthetic Purposes | NFO | Class 2 | Neurology | No | 2018-01-03 |
| Electrocardiograph, Ambulatory (Without Analysis) | MWJ | Class 2 | Cardiovascular | No | 2025-12-31 |
| Pump, Infusion | FRN | Class 2 | General Hospital | No | 2025-12-26 |
Proprietary Names
Nubody Skin Toning Device
KIP II+
Establishment Types
Manufacture Medical Device for Another Party (Contract Manufacturer)