BENCOX Hip System

FDA UDI

Class II (US FDA UDI)

by Corentec Co., Ltd

Identity

Trade Name: BENCOX Hip System FDA UDI
Generic Name: Non-constrained polyethylene acetabular liner FDA UDI
Device Name: Bencox Mirabo PE Liner-10° Elevated type(Type A) (GUR1050) FDA UDI
Model / Reference: H1.L67.4062 FDA UDI
Description: Bencox Mirabo PE Liner-10° Elevated type(Type A) (GUR1050) FDA UDI

Identifiers

Primary DI / UDI-DI: 08800017220260 FDA UDI
510(k) Number: K162127 FDA UDI
K172806 FDA UDI
FDA Product Code: LZO FDA UDI
KWY FDA UDI
LPH FDA UDI
GMDN Term: Non-constrained polyethylene acetabular liner FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3353 FDA UDI
888.3390 FDA UDI
888.3358 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Non-constrained polyethylene acetabular liner

BENCOX Hip System by Corentec Co., Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-constrained polyethylene acetabular liner.

C-Fit & DC-Fit Acetabular Cup System — CORIN LTD · Class II
RINGLOC HIP SYSTEM — Biomet Orthopedics, Inc. · Class II
MobileLink Acetabular Cup System — WALDEMAR LINK GmbH & Co. KG · Class II
PRIME — MicroPort Orthopedics Inc. · Class II
G7 Acetabular Liner — Biomet Orthopedics, Inc. · Class II
Logical 20° Hooded Liner — SIGNATURE ORTHOPAEDICS PTY LTD · Class II
RINGLOC RX90-2 HIP SYSTEM — Biomet Orthopedics, Inc. · Class II
PINNACLE — DEPUY ORTHOPAEDICS, INC. · Class II

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Corentec Co., Ltd

Sources (1)

FDA UDI ac3886c5-1b97-4edd-b2bc-820da3b95576 35 fields · synced May 31, 2026