FDA Registration Active 🇺🇸 United States

SLR-PLUS REVISION STEM LATERAL 4 NON-CEM

Reg #: 3002907620 · FEI: 3002907620 · Expires 2025
Products
1
Proprietary Names
22
Establishment Types
1
Classifications
1

Registration Details

Registration Name
Sterigenics US LLC
Registration Number
3002907620
FEI Number
3002907620
Status
Active
Expiry Year
2025
Initial Importer
No
Address
1700 College Blvd.
City
West Memphis
State
AR
ZIP
72301
Country
US

Regulatory Submissions

510(k) Number
K093991

Owner / Operator

Firm Name
Sotera Health LLC
Operator Number
10029425
Address
2015 Spring Road, Suite 650
City
Oak Brook
State
IL
Postal Code
60523
Country
US
Correspondent
Karen Whaley-Krumins

Products

Device Name Product Code
Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented LZO

Proprietary Names

SLR-PLUS REVISION STEM LATERAL 4 NON-CEM SLR-PLUS REVISION STEM 3 NON-CEMENTED SLR-PLUS REVISION STEM 10 NON-CEMENTED SLR-PLUS REVISION STEM 6 NON-CEMENTED SLR-PLUS REVISION STEM LATERAL 8 NON-CEM SLR-PLUS REVISION STEM LATERAL 10NON-CEM SLR-PLUS REVISION STEM 2 NON-CEMENTED SLR-PLUS REVISION STEM 11 NON-CEMENTED SLR-PLUS REVISION STEM LATERAL 5 NON-CEM SLR-PLUS REVISION STEM 5 NON-CEMENTED SLR-PLUS REVISION STEM LATERAL 2 NON-CEM SLR-PLUS REVISION STEM LATERAL 9 NON-CEM SLR-PLUS REVISION STEM 8 NON-CEMENTED SLR-PLUS REVISION STEM LATERAL 3 NON-CEM SLR-PLUS REVISION STEM 1 NON-CEMENTED SLR-PLUS REVISION STEM LATERAL 11NON-CEM SLR-PLUS REVISION STEM LATERAL 1 NON-CEM SLR-PLUS REVISION STEM 9 NON-CEMENTED SLR-PLUS REVISION STEM LATERAL 7 NON-CEM SLR-PLUS REVISION STEM LATERAL 6 NON-CEM SLR-PLUS REVISION STEM 4 NON-CEMENTED SLR-PLUS REVISION STEM 7 NON-CEMENTED

Establishment Types

Sterilize Medical Device for Another Party (Contract Sterilizer)