FDA Registration
Active
🇺🇸 United States
Cannula, Curved, 5x300mm, Camera Right
Reg #: 3009161688
·
FEI: 3009161688
·
Expires 2025
Products
1
Proprietary Names
12
Establishment Types
1
Classifications
1
Registration Details
- Registration Name
- VERIDIAM, INC
- Registration Number
- 3009161688
- FEI Number
- 3009161688
- Status
- Active
- Expiry Year
- 2025
- Initial Importer
- No
- Address
- 1717 North Cuyamaca Street
- City
- El Cajon
- State
- CA
- ZIP
- 92020
- Country
- US
Owner / Operator
- Firm Name
- Veridiam, Inc
- Operator Number
- 10046309
- Address
- 1717 North Cuyamaca Street
- City
- El Cajon
- State
- CA
- Postal Code
- 92020
- Country
- US
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Cannula, Surgical, General & Plastic Surgery | GEA | Class 1 | General, Plastic Surgery | No | 2017-10-26 |
Proprietary Names
Cannula, Curved, 5x300mm, Camera Right
Cannula, Curved, 5x250mm, Camera Left
Accessory Cannula, 5mm, Single Site
Cannula, Curved, 5x250mm, Camera Right
Cannula, Curved, 5x300mm, Camera Left
Cannula, 12mm & Stapler, Long, Reusable
Cannula, 12mm & Stapler, Standard, Reusable
Cannula, 8mm, Standard, Reusable
Cannula, 12mm, Long, Reusable
Cannula, 8mm, Long, Reusable
Cannula, 8mm, Flared-Grounded, Reusable
Cannula, 8mm, Grounded, Camera, Single Site
Establishment Types
Manufacture Medical Device for Another Party (Contract Manufacturer)