Onvoy

ONVOY Acetabular EXp+ Liner, Lateralized, 36mm ID, 54-56 OD

Registry build 21.09.26
14manufacturers in China registered for this device type
59catalogue numbers in this listing
4510(k) clearances naming this product code

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 Onvoy
Listed by Globus Medical, Inc., United States
FDA product code LPH
Device type Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
Device class Class 2
Regulation 21 CFR 888.3358
Establishment Manufacturer, Exporter
510(k) K213842
Record published 2023-01-24
Record revised 2023-05-03 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for Onvoy
Catalogue number Size Status
4235.4146S In distribution
4235.1372S In distribution
4235.4354S In distribution
4235.3250S In distribution
1235.0460S In distribution
5235.5400S In distribution
4235.8048S In distribution
4235.4150S In distribution
1235.0152S In distribution
4235.5354S In distribution
4235.4350S In distribution
4235.2262S In distribution
1235.0162S In distribution
4235.1166S In distribution
4235.4254S In distribution
4235.5154S In distribution
4235.5466S In distribution
4235.1358S In distribution
4235.8150S In distribution
4235.4358S In distribution
1235.0454S In distribution
4235.5462S In distribution
4235.8058S In distribution
4235.3254S In distribution
4235.4250S In distribution
4235.3366S In distribution
4235.2250S In distribution
1235.0154S In distribution
6235.0310 In distribution
4235.3154S In distribution
4235.5266S In distribution
4235.4258S In distribution
1235.0452S In distribution
1235.1340S In distribution
1235.0468S In distribution
1235.0164S In distribution
4235.5358S In distribution
4235.4262S In distribution
4235.2158S In distribution
4235.3354S In distribution
4235.3266S In distribution
4235.3158S In distribution
1235.1320S In distribution
4235.8066S In distribution
1235.0166S In distribution
4235.5254S In distribution
4235.5350S In distribution
1235.1335S In distribution
4235.3150S In distribution
4235.2254S In distribution
1235.0148S In distribution
4235.1362S In distribution
4235.3258S In distribution
4235.3362S In distribution
4235.8050S In distribution
4235.4142S In distribution
4235.4158S In distribution
1235.0158S In distribution
4235.4266S 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

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K254043 2026-08-04
K243456 2025-06-06
K213842 2022-10-03
K201733 2021-07-14

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