← Back to catalogue

BENCOX Hip System

FDA UDI

Class II (US FDA UDI)

by Corentec Co., Ltd

Identity

Trade Name
BENCOX Hip System FDA UDI
Generic Name
Press-fit femoral stem prosthesis FDA UDI
Device Name
BENCOX II STEM(Blasting) FDA UDI
Model / Reference
01.01.907 FDA UDI
Description
BENCOX II STEM(Blasting) FDA UDI

Identifiers

Primary DI / UDI-DI
08806373833359 FDA UDI
510(k) Number
K103431 FDA UDI
K120924 FDA UDI
K122099 FDA UDI
FDA Product Code
KWY FDA UDI
LPH FDA UDI
GMDN Term
Press-fit femoral stem prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Press-fit femoral stem prosthesis

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

Similar devices

Also classified as Press-fit femoral stem prosthesis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Corentec Co., Ltd

Sources (1)

  • FDA UDI 495a8f82-27ce-4dfd-aebf-0a06ba39284b 35 fields · synced May 30, 2026