Vento Xlpe Liner

56 catalogue numbers from 1-01-12-7456, listed by Amplitude, France, under Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented. 14 manufacturers in China are registered for this product code.

Registry build 21.09.26
14manufacturers in China registered for this device type
56catalogue numbers in this listing

Who Else Makes It

Concentrated in Jiangsu (7), Shanghai (3), Zhejiang (2). 10 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code LPH
Manufacturer City Province Registered as Device types
MicroPort Orthopedics Global Supply Center Limited Shanghai Shanghai Contract manufacturer 82
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Canwell Medical Co., Ltd. Jinhua Zhejiang Contract manufacturer 42
Suzhou Elite Precision Machinery Co., Ltd. Kunshan Jiangsu Contract manufacturer 35
Guangzhou Aquila Precise Tools Limited Guangzhou Guangdong Contract manufacturer 28
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
APS Materials Suzhou Suzhou Jiangsu Contract manufacturer 18
Xian Airfoil Technology Co., Ltd. Xian Shaanxi Contract manufacturer 8
Lincotek (Wuxi) Co., Ltd. Wuxi Jiangsu Contract manufacturer 7
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70

Showing 12 of 14. All 14 manufacturers in China registered for Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

Record

Regulatory record for Vento Xlpe Liner
Listed by Amplitude, France
FDA product code LPH
Device type Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
Device class Class 2
Regulation 21 CFR 888.3358
Establishment Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K121297
Record published 2017-12-18
Record revised 2018-07-06 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date

Catalogue Numbers

Catalogue numbers for Vento Xlpe Liner
Catalogue number Size Status
1-01-12-7456 In distribution
1-01-12-5250 In distribution
1-01-12-5844 In distribution
1-01-12-8456 In distribution
1-01-12-7256 In distribution
1-01-12-9202 In distribution
1-01-12-7656 In distribution
1-01-12-8652 In distribution
1-01-12-8460 In distribution
1-01-12-0250 In distribution
1-01-12-8252 In distribution
1-01-12-8250 In distribution
1-01-12-0460 In distribution
1-01-12-6250 In distribution
1-01-12-0660 In distribution
1-01-12-6256 In distribution
1-01-12-8660 In distribution
1-01-12-5850 In distribution
1-01-12-5256 In distribution
1-01-12-6652 In distribution
1-01-12-6252 In distribution
1-01-12-8844 In distribution
1-01-12-9204 In distribution
1-01-12-8260 In distribution
1-01-12-6460 In distribution
1-01-12-8656 In distribution
1-01-12-0256 In distribution
1-01-12-0850 In distribution
1-01-12-6850 In distribution
1-01-12-5656 In distribution
1-01-12-8256 In distribution
1-01-12-0652 In distribution
1-01-12-7250 In distribution
1-01-12-5852 In distribution
1-01-12-8850 In distribution
1-01-12-5260 In distribution
1-01-12-5652 In distribution
1-01-12-5660 In distribution
1-01-12-5460 In distribution
1-01-12-7850 In distribution
1-01-12-6844 In distribution
1-01-12-7660 In distribution
1-01-12-7260 In distribution
1-01-12-6660 In distribution
1-01-12-7652 In distribution
1-01-12-7844 In distribution
1-01-12-8852 In distribution
1-01-12-7460 In distribution
1-01-12-6656 In distribution
1-01-12-6260 In distribution
1-01-12-5456 In distribution
1-01-12-5252 In distribution
1-01-12-7252 In distribution
1-01-12-7852 In distribution
1-01-12-6852 In distribution
1-01-12-6456 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Initia Total Hip System Kyocera Medical Technologies, Inc. 1,000
DJO Surgical Encore Medical, L.P. 624
Pinnacle Depuy Orthopaedics, Inc. 613
Trilogy® Longevity® Zimmer, Inc. 564
Instrument Howmedica Osteonics Corp 369
InSitu Hip System Nextstep Arthropedix 368
Trilogy® Zimmer, Inc. 359
Kyocera Medical Technologies, Inc. Kyocera Medical Technologies, Inc. 298
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented Zimmer, Inc. 286
Bencox Hip System Corentec Co., Ltd. 286
OrthoMedFlex Orthomedflex LLC 257
Sterizo Total Hip System CPM Medical Consultants, LLC. 240

Showing 12 of 792. All products under Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P880025 1991-12-04 AML(R) POROCOAT(R) ACETABULAR CUP PROSTHESIS Depuy Intl., Ltd.
P880076 1991-06-17 WHITESIDE EPS(TM) FEMORAL HIP PROSTHESIS Dow Corning Wright
P850061 1991-03-08 BIAS(R) FIBER METAL TOTAL HIP SYSTEM Zimmer, Inc.

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer