FDA Registration
Active
🇺🇸 United States
MiroDerm Fenestrated Plus
Reg #: 3010894343
·
FEI: 3010894343
·
Expires 2025
Products
1
Proprietary Names
2
Establishment Types
1
Classifications
1
Registration Details
- Registration Name
- Reprise Biomedical, Inc.
- Registration Number
- 3010894343
- FEI Number
- 3010894343
- Status
- Active
- Expiry Year
- 2025
- Initial Importer
- No
- Address
- 17400 Medina Road, Suite 100
- City
- Plymouth
- State
- MN
- ZIP
- 55447
- Country
- US
Regulatory Submissions
- 510(k) Number
- K143426
Owner / Operator
- Firm Name
- Reprise Biomedical
- Operator Number
- 10078738
- Address
- 17400 Medina Road, Suite 100
- City
- Plymouth
- State
- MN
- Postal Code
- 55447
- Country
- US
- Correspondent
- Carrie Powers
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Wound Dressing With Animal-Derived Material(S) | KGN | Class U | Unknown | No | 2020-11-03 |
Proprietary Names
MiroDerm Fenestrated Plus
MiroDerm Fenestrated
Establishment Types
Manufacture Medical Device