Vanguard® Vivacit-E®

68 catalogue numbers from VE183644, listed by Zimmer, Inc., United States, under Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive. 8 manufacturers in China are registered for this product code.

Registry build 21.09.26
8manufacturers in China registered for this device type
68catalogue numbers in this listing
1recall

Who Else Makes It

Concentrated in Jiangsu (4), Shanghai (2), Zhejiang (1). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code OIY
Manufacturer City Province Registered as Device types
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
b-ONE Medical (Beijing) Co., Ltd. Beijing Beijing 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
Steris Sterilization Technologies (Suzhou) Ltd Suzhou Jiangsu Contract manufacturer 44
Johnson & Johnson Medical (Depuy – Suzhou) Ltd. Suzhou Jiangsu Manufacturer 34

Record

Regulatory record for Vanguard® Vivacit-E®
Listed by Zimmer, Inc., United States
FDA product code OIY
Device type Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive
Device class Class 2
Regulation 21 CFR 888.3560
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Manufacturer, Exporter
510(k) K183583
Record published 2019-10-11

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Sizes Width 59 to 91 mm

Catalogue Numbers

Catalogue numbers for Vanguard® Vivacit-E®
Catalogue number Size Status
VE183644 14 mm, Thickness In distribution
VE183628 Width 67.00 mm In distribution
VE189141 11 mm, Thickness In distribution
VE183408 Width 59.00 mm In distribution
VE189100 10 mm, Thickness In distribution
VE183481 Width 91.00 mm In distribution
VE183760 Width 79.00 mm In distribution
VE183406 16 mm, Thickness In distribution
VE183668 18 mm, Thickness In distribution
VE189021 11 mm, Thickness In distribution
VE189128 18 mm, Thickness In distribution
VE183604 14 mm, Thickness In distribution
VE189028 18 mm, Thickness In distribution
VE183648 Width 71.00 mm In distribution
VE183621 11 mm, Thickness In distribution
VE183483 Width 87.00 mm In distribution
VE189088 Width 75.00 mm In distribution
VE189101 Width 79.00 mm In distribution
VE183464 Width 83.00 mm In distribution
VE183724 Width 63.00 mm In distribution
VE183448 18 mm, Thickness In distribution
VE183603 13 mm, Thickness In distribution
VE183586 16 mm, Thickness In distribution
VE183566 Width 79.00 mm In distribution
VE183680 10 mm, Thickness In distribution
VE189043 Width 67.00 mm In distribution
VE183646 Width 71.00 mm In distribution
VE189008 Width 59.00 mm In distribution
VE189121 11 mm, Thickness In distribution
VE189060 10 mm, Thickness In distribution
VE183600 10 mm, Thickness In distribution
VE183748 Width 71.00 mm In distribution
VE189104 Width 79.00 mm In distribution
VE183463 13 mm, Thickness In distribution
VE189122 Width 83.00 mm In distribution
VE189148 Width 87.00 mm In distribution
VE183421 11 mm, Thickness In distribution
VE183541 11 mm, Thickness In distribution
VE189081 11 mm, Thickness In distribution
VE183782 12 mm, Thickness In distribution
VE183768 Width 79.00 mm In distribution
VE183664 Width 83.00 mm In distribution
VE183642 12 mm, Thickness In distribution
VE189001 Width 59.00 mm In distribution
VE183762 12 mm, Thickness In distribution
VE183401 Width 59.00 mm In distribution
VE183744 Width 71.00 mm In distribution
VE183442 Width 75.00 mm In distribution
VE183520 Width 63.00 mm In distribution
VE189046 Width 67.00 mm In distribution
VE183523 Width 67.00 mm In distribution
VE183480 Width 91.00 mm In distribution
VE183488 Width 87.00 mm In distribution
VE183526 Width 67.00 mm In distribution
VE183446 Width 71.00 mm In distribution
VE183606 Width 59.00 mm In distribution
VE183542 12 mm, Thickness In distribution
VE183588 Width 91.00 mm In distribution
VE189144 14 mm, Thickness In distribution
VE189083 Width 75.00 mm In distribution
VE189140 Width 87.00 mm In distribution
VE189020 10 mm, Thickness In distribution
VE189126 Width 83.00 mm In distribution
VE183466 Width 83.00 mm In distribution
VE189062 Width 71.00 mm In distribution
VE183662 12 mm, Thickness In distribution
VE189022 Width 63.00 mm In distribution
VE183663 13 mm, Thickness In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Persona® Zimmer, Inc. 552
DJO Surgical Encore Medical, L.P. 415
Genflex2 Total Knee System Globus Medical, Inc. 389
Persona® Vivacit-E® Zimmer, Inc. 332
Truliant, Activit-E Exactech, Inc. 272
TriVerse Meniscal Insert PS Signature Orthopaedics PTY Limited 220
U2™ Knee United Orthopedic Corp. 195
BKS E-Vitalize Ortho Development Corp. 193
Vanguard XP Instrumentation Biomet Orthopedics 169
Attune Depuy (Ireland) 161
Vanguard Complete Knee System Biomet Orthopedics 153
EXp Tibial Inserts and Patellar Components Globus Medical, Inc. 144

Showing 12 of 102. All products under Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive

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
2014-12-11 Class II Device Design Potential for delay in surgery and/or ball bearings to be left in the wound. Repeated cycles of sonic cleaning can break down the ball bearing retention feature (swage) on the shim. To prevent this, TASP shims must be manually cleaned and i 67963 2015-10-23

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