FDA Registration
Active
🇺🇸 United States
MaxiFlex Laser Fiber
Reg #: 3006812215
·
FEI: 3006812215
·
Expires 2025
Products
1
Proprietary Names
1
Establishment Types
2
Classifications
1
Registration Details
- Registration Name
- MAXIFLEX, LLC
- Registration Number
- 3006812215
- FEI Number
- 3006812215
- Status
- Active
- Expiry Year
- 2025
- Initial Importer
- No
- Address
- 512 Verret St
- City
- New Orleans
- State
- LA
- ZIP
- 70114
- Country
- US
Regulatory Submissions
- 510(k) Number
- K013300
Owner / Operator
- Firm Name
- MAXIFLEX, LLC
- Operator Number
- 9048007
- Address
- 512 Verret st
- City
- New Orleans
- State
- LA
- Postal Code
- 70114
- Country
- US
- Correspondent
- GARY - VENTRELLA
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Powered Laser Surgical Instrument | GEX | Class 2 | General, Plastic Surgery | No | 2003-06-30 |
Proprietary Names
MaxiFlex Laser Fiber
Establishment Types
Manufacture Device in the United States for Export Only
Complaint File Establishment per 21 CFR 820.198