FDA Registration
Active
🇺🇸 United States
PATHWAY MEDTECH, LLC.
Reg #: 3012833053
·
FEI: 3012833053
·
Expires 2026
Products
9
Proprietary Names
0
Establishment Types
3
Classifications
9
Registration Details
- Registration Name
- PATHWAY MEDTECH, LLC.
- Registration Number
- 3012833053
- FEI Number
- 3012833053
- Status
- Active
- Expiry Year
- 2026
- Initial Importer
- No
- Address
- 8779 Cottonwood Ave Ste 105
- City
- Santee
- State
- CA
- ZIP
- 92071
- Country
- US
Owner / Operator
- Firm Name
- Pathway Medtech, LLC.
- Operator Number
- 10052260
- Address
- 8779 Cottonwood Ave, Suite 105
- City
- Santee
- State
- CA
- Postal Code
- 92071
- Country
- US
- Correspondent
- Arthur Deptala
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Instrument, Surgical, Non-Powered | HAO | Class 1 | Neurology | No | 2024-11-21 |
| Catheter, Septostomy | DXF | Class 2 | Cardiovascular | No | 2025-02-19 |
| Tape And Bandage, Adhesive | KGX | Class 1 | General Hospital | No | 2023-11-10 |
| Syringe, Piston | FMF | Class 2 | General Hospital | No | 2023-11-10 |
| Ligator, Hemorrhoidal | FHN | Class 2 | Gastroenterology, Urology | No | 2020-11-17 |
| Catheter, Ultrasound, Intravascular | OBJ | Class 2 | Cardiovascular | No | 2025-12-03 |
| Accessories, Catheter | KGZ | Class 1 | General, Plastic Surgery | No | 2024-10-17 |
| Container, Specimen Mailer And Storage, Non-Sterile | NNK | Class 1 | Pathology | No | 2022-10-18 |
| Catheter, Retention Type, Balloon | EZL | Class 2 | Gastroenterology, Urology | No | 2020-11-03 |
Establishment Types
Manufacture Medical Device for Another Party (Contract Manufacturer)
Repack or Relabel Medical Device
Manufacture Medical Device