Corentec Co., Ltd.
Corentec Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2010, most recent 2025, with 3 FDA device recalls on record.
Top product codes for Corentec Co., Ltd.
FDA recalls by Corentec Co., Ltd.
- Z-1935-2024 — LOSPA Patella Component Model/Catalog Number: 01.10.9XX Software Version: N/A Product Description: Patella
- Z-1934-2024 — LOSPA Tibial Insert Model/Catalog Number: See below Software Version: N/A Product Description: Tibial Insert
- Z-1454-2017 — Bencox Mirabo PE Liner 36/44 Model Number: H1.L61.3644, UDI: 8806373852343
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Corentec Co., Ltd.
- K250889 — EXULT Knee Replacement System
- K242401 — EXULT Knee Replacement System
- K242046 — EXULT Knee Replacement System
- K223828 — BENCOX Delta Option Heads
- K223223 — BENCOX Mirabo Z Cup Cortinium
- K222278 — LOSPA TKR System Instrumentation, EXULT TKR System Instrumentation
- K210614 — BENCOX Mirabo Z Cup Cortinium
- K220468 — BENCOX Mirabo Cup System
- K212034 — LOSPA TKR System
- K211866 — Bencox THR System
- K201851 — EXULT Femoral component trial - Left, EXULT Femoral component trial - Right
- K200395 — LOSPA II Knee System (EXULT Knee Replacement System)
- K200267 — LOSPA® IS Spinal Fixation System
- K192507 — LOSPA II Knee System
- K182221 — Bencox Mirabo Cup Multi Hole
- K172806 — Bencox Mirabo Cup System
- K170243 — LOSPA IS TLIF & DLIF Cages
- K161641 — LOSPA IS ACP System
- K162127 — Bencox M Stem Lateralized & Bencox Mirabo Cup System
- K160157 — LOSPA Modular Knee System
- K152084 — Bencox M Stem (Bencox Hip System) and Bencox ID Cemented Stem (with Centralizer) & Bencox Bone Plug
- K151408 — LOSPA IS Spinal System
- K150007 — Modified Bencox Hip System
- K132644 — LOSPA IS PEDICLE SCREW (MONOAXIAL & POLYAXIAL), LOSPA IS ROD- STRAIGHT (STANDARD), LOSPA IS ROD- PRE BENT (STANDARD & BU
- K130673 — LOSPA TOTAL KNEE REPLACEMENT SYSTEM
- K122099 — BENCOX II STEM, BENCOX METAL HEAD
- K121665 — BENCOX FORET & BENCOX DELTA
- K120924 — BENCOX MIRABO CUP BENCOX MIRABO INSERT (STANDARD& ELEVATED TYES) BENCOX MIRABO CUP SCREW HOLE PLUG
- K121037 — LOSPA TIBIAL BASE PLATE
- K110404 — EAUM TOTAL KNEE SYSTEM
- K112019 — BENCOX ID STEM, BENCOX METAL HEAD, BENCOX BIPOLAR CUP
- K103431 — COREN TOTAL HIP SYSTEM
- K092076 — AEGIS & AEGIS II SPINAL SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.