Onvoy

ONVOY Acetabular EXp+ Liner, Lateralized, 28mm ID, 50-52 OD

Registry build 21.09.26
8manufacturers in China registered for this device type
48catalogue numbers in this listing
1recall

Who Else Makes It

Concentrated in Shanghai (3), Jiangsu (3), Zhejiang (1). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code OQG
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
APS Materials Suzhou Suzhou Jiangsu Contract manufacturer 18
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
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
Shenzhen Fox Hunting E-commerce Co., Ltd. Shenzhen Guangdong Exporter 7

Record

Regulatory record for Onvoy
Listed by Globus Medical, Inc., United States
FDA product code OQG
Device type Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented
Device class Class 2
Regulation 21 CFR 888.3358
Establishment Manufacturer, Exporter
510(k) K213842
Record published 2023-01-24
Record revised 2024-02-19 (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
1235.0156S In distribution
4235.1142S In distribution
4235.3350S In distribution
1235.0160S In distribution
4235.2154S In distribution
4235.1266S In distribution
4235.5150S In distribution
1235.1315S In distribution
1235.1325S In distribution
5235.5404S In distribution
1235.0446S In distribution
4235.2458S In distribution
4235.1272S In distribution
1235.0144S In distribution
4235.5166S In distribution
4235.8166S In distribution
4235.2258S In distribution
4235.1146S In distribution
4235.3358S In distribution
4235.3142S In distribution
4235.4162S In distribution
4235.2150S In distribution
1235.0470S In distribution
4235.2362S In distribution
4235.4246S In distribution
1235.0150S In distribution
4235.4154S In distribution
1235.1350S In distribution
4235.2142S In distribution
4235.5262S In distribution
4235.5142S In distribution
1235.0474S In distribution
4235.5162S In distribution
1235.0458S In distribution
4235.1466S In distribution
4235.2462S In distribution
4235.5148S In distribution
4235.1454S In distribution
1235.0464S In distribution
6235.0301 In distribution
4235.1350S In distribution
4235.1254S In distribution
4235.5158S In distribution
4235.2472S In distribution
4235.5246S In distribution
4235.2354S In distribution
1235.0450S In distribution
4235.8154S In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
CS2 Acet. Cup Sys. – VitalitE Shalby Advanced Technologies, Inc. 169
iTotal® Hip Replacement System ConforMIS, Inc. 131
CS2 Acet. Cup Sys. – VitalitE Consensus Orthopedics, Inc. 124
DJO Surgical Encore Medical, L.P. 99
MobileLink Acetabular Cup System Waldemar Link GmbH & Co. KG 68
G7 Biomet Orthopedics 54
Vitelene® Aesculap AG 52
Conformis Hip System ConforMIS, Inc. 51
Ringloc HIP System Biomet Orthopedics 35
Novosource Total Hip System Novosource, LLC 33
Prime Microport Orthopedics Inc. 32
NovoHip Total Hip System Novosource, LLC 28

Showing 12 of 100. All products under Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented

Recalls

1 of these is Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2013-01-24 Class II Device Design Firm was made aware of incidents relating to the difficulty of properly engaging and securing the Cross-Over 36mm liner into the Cross-Over shell. 254 2014-10-08

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