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
Wound Dressing With Animal-Derived Material(S) KGN

Proprietary Names

MiroDerm Fenestrated Plus MiroDerm Fenestrated

Establishment Types

Manufacture Medical Device