Corentec Co., Ltd. - FDA 510(k) Cleared Devices
33
Total
33
Cleared
0
Denied
Corentec Co., Ltd. has 33 FDA 510(k) cleared orthopedic devices. Based in West Cadwell, US.
Latest FDA clearance: Apr 2025. Active since 2010.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
33 devices
Cleared
Apr 17, 2025
EXULT Knee Replacement System
Orthopedic
23d
Cleared
Sep 12, 2024
EXULT Knee Replacement System
Orthopedic
30d
Cleared
Aug 01, 2024
EXULT Knee Replacement System
Orthopedic
20d
Cleared
Mar 16, 2023
BENCOX Delta Option Heads
Orthopedic
85d
Cleared
Feb 27, 2023
BENCOX Mirabo Z Cup Cortinium
Orthopedic
133d
Cleared
Aug 26, 2022
LOSPA TKR System Instrumentation, EXULT TKR System Instrumentation
Orthopedic
28d
Cleared
May 24, 2022
BENCOX Mirabo Z Cup Cortinium
Orthopedic
449d
Cleared
May 18, 2022
BENCOX Mirabo Cup System
Orthopedic
90d
Cleared
Dec 09, 2021
LOSPA TKR System
Orthopedic
163d
Cleared
Jul 14, 2021
Bencox THR System
Orthopedic
28d
Cleared
Jul 30, 2020
EXULT Femoral component trial - Left, EXULT Femoral component trial - Right
Orthopedic
24d
Cleared
May 07, 2020
LOSPA II Knee System (EXULT Knee Replacement System)
Orthopedic
79d