Vanguard®

106 catalogue numbers from 32-489061, listed by Biomet Orthopedics, United States, under Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer. 21 manufacturers in China are registered for this product code.

Registry build 21.09.26
21manufacturers in China registered for this device type
106catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (10), Shanghai (4), Beijing (3). 13 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code JWH
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
B-ONE Medical (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 23
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Stryker Orthmed (Changzhou) Medical Instrument Co., Ltd. Changzhou Jiangsu Contract manufacturer 10
b-ONE Medical (Beijing) Co., Ltd. Beijing Beijing Contract manufacturer 7
Changzhou Wastonortho Medical Appliance Co., Ltd. Changzhou Jiangsu Contract manufacturer 5

Showing 12 of 21. All 21 manufacturers in China registered for Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Record

Regulatory record for Vanguard®
Listed by Biomet Orthopedics, United States
FDA product code JWH
Device type Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Device class Class 2
Regulation 21 CFR 888.3560
510(k) K113550
Record published 2021-03-24
Record revised 2025-05-30 (version 13)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Prescription Prescription only
Label carries lot or batch number, manufacturing date
Sizes Width 67 to 83 mm; height 10 to 18 mm; length 63 to 79 mm

Catalogue Numbers

Catalogue numbers for Vanguard®
Catalogue number Size Status
32-489061 11 mm X 71 mm In distribution
32-489034 24 mm X 63 mm In distribution
32-489144 14 mm X 87 mm In distribution
32-489090 20 mm X 75 mm In distribution
32-489121 11 mm X 83 mm In distribution
32-483804 14 mm X 59 mm In distribution
32-489008 18 mm X 59 mm In distribution
32-489040 10 mm X 67 mm In distribution
32-489143 13 mm X 87 mm In distribution
SSI002495 Width 83 mm In distribution
32-489023 13 mm X 63 mm In distribution
SSI001051 65 R In distribution
SSI002489 Width 75 mm In distribution
599301 In distribution
32-483862 12 mm X 79/83 mm In distribution
SSI002481 Width 67 mm In distribution
SSI004864 14×87/91 mm In distribution
SSI001055 70 R In distribution
32-489083 13 mm X 75 mm In distribution
32-489021 11 mm X 63 mm In distribution
32-483004 60 mm In distribution
32-360514 24MM X 59MM In distribution
SSI002483 Width 67 mm In distribution
SSI002103 71/75 mm Width x 10 mm Height In distribution
32-489086 16 mm X 75 mm In distribution
32-360510 20MM X 59MM In distribution
SSI002101 63/67 mm Width x 12 mm Height In distribution
SSI002494 Length 79 mm In distribution
SSI002488 Length 71 mm In distribution
32-483866 16 mm X 79/83 mm In distribution
32-483108 65 mm In distribution
32-483034 75 mm In distribution
32-489052 22 mm X 67 mm In distribution
SSI002130 Width 75 mm In distribution
599305 In distribution
32-483894 24 mm X 87/91 mm In distribution
SSI002492 Length 79 mm In distribution
32-483850 20 mm X 71/75 mm In distribution
32-483900 In distribution
32-489100 10 mm X 79 mm In distribution
SSI001047 60 R In distribution
SSI002491 Width 83 mm In distribution
32-489001 11 mm X 59 mm In distribution
32-489084 14 mm X 75 mm In distribution
32-489114 24 mm X 79 mm In distribution
32-483012 70 mm In distribution
SSI002105 71/75 mm Width x 14 mm Height In distribution
32-360504 14MM X 59MM In distribution
32-489066 16 mm X 71 mm In distribution
32-483132 70 mm In distribution
32-483886 16MM X 87/91MM In distribution
32-489064 14 mm X 71 mm In distribution
32-489062 12 mm X 71 mm In distribution
SSI002484 Length 63 mm In distribution
32-489054 24 mm X 67 mm In distribution
32-360102 In distribution
SSI001060 75 R In distribution
32-483704 14 mm X 59 mm In distribution
32-483006 62.5 mm In distribution
SSI002490 Length 71 mm In distribution
32-483102 57.5 mm In distribution
SSI002485 Width 67 mm In distribution
32-489032 22 mm X 63 mm In distribution
32-489024 14 mm X 63 mm In distribution
32-483866 16MM X 79/83MM In distribution
32-489141 11 mm X 87 mm In distribution
32-486535 40 mm In distribution
SSI004860 12×59 mm In distribution
SSI002107 79/83 mm Width x 12 mm Height In distribution
32-483894 24MM X 87/91MM In distribution
599308 In distribution
SSI002482 Length 63 mm In distribution
32-489003 13 mm X 59 mm In distribution
32-483033 72.5 mm In distribution
32-489146 16MM X 87MM In distribution
32-360512 22MM X 59MM In distribution
32-483874 24 mm X 79/83 mm In distribution
32-489142 12MM X 87MM In distribution
32-483888 18MM X 87/91MM In distribution
SSI002487 Width 75 mm In distribution
32-483036 80 mm In distribution
32-489146 16 mm X 87 mm In distribution
32-360101 In distribution
SSI002486 Length 71 mm In distribution
SSI004862 10×87/91 mm In distribution
32-483702 12 mm X 59 mm In distribution
SSI001049 62.5 R In distribution
32-360108 5MM In distribution
32-483854 24 mm X 71/75 mm In distribution
32-489102 12 mm X 79 mm In distribution
32-483848 18 mm X 71/75 mm In distribution
32-489128 18 mm X 83 mm In distribution
32-483864 14 mm X 79/83 mm In distribution
32-489020 10 mm X 63 mm In distribution
32-489106 16 mm X 79 mm In distribution
SSI001053 67.5 R In distribution
32-360502 12MM X 59MM In distribution
SSI002493 Width 83 mm In distribution
32-486530 25 mm In distribution
32-483008 65 mm In distribution
32-483128 65 mm In distribution
32-483010 67.5 mm In distribution
32-483028 65 mm In distribution
599305 In distribution
32-483782 12 mm X 87/91 mm In distribution
32-486534 37 mm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Prophecy® Microport Orthopedics Inc. 4,423
Exult Knee Replacement System Corentec Co., Ltd. 1,770
Freedom Maxx Orthopedics Inc. 1,693
Legion Smith & Nephew, Inc. 1,534
MyKnee Medacta International SA 1,466
Journey Smith & Nephew, Inc. 1,339
Persona® Zimmer, Inc. 1,254
DJO Surgical Encore Medical, L.P. 1,131
U2 Total Knee System United Orthopedic Corp. 1,078
CKS Plus Shalby Advanced Technologies, Inc. 1,024
Lospa Modular Knee System Corentec Co., Ltd. 1,020
Natural-Knee® Zimmer, Inc. 980

Showing 12 of 1,175. All products under Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K080528 2008-06-17
K022586 2002-08-15

Recalls Naming This Product

12 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of Vanguard®
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Biomet, Inc. 510(k) number 2022-12-29 Class II Labeling Change Control Components Incorrectly labeled as either smaller or larger and incorrect side (right/left). 157 units
Biomet, Inc. 510(k) number 2022-12-29 Class II Labeling Change Control Components Incorrectly labeled as either smaller or larger and incorrect side (right/left). 91 units
Biomet, Inc. 510(k) number 2020-12-01 Class II Process control Incorrect bolt -tibial bolts in package instead of femoral bolts may delay procedure 21 units 2022-07-08
Biomet, Inc. 510(k) number 2018-10-22 Class II Labeling mix-ups Label on the outer carton or the patient labels does not match label on the inner sterile packaging 8 units 2019-12-11
Biomet, Inc. 510(k) number 2018-10-22 Class II Labeling mix-ups Label on the outer carton or the patient labels does not match label on the inner sterile packaging 8 units 2019-12-11
Biomet, Inc. 510(k) number 2018-08-02 Class II Under Investigation by firm The implant only has one bolt in the sterile package but it should have had two. 16 2019-04-25
Biomet, Inc. 510(k) number 2018-08-02 Class II Under Investigation by firm The implant only has one bolt in the sterile package but it should have had two. 16 2019-04-25
Biomet, Inc. 510(k) number 2018-05-24 Class II Under Investigation by firm Two lots of tibial bearings were commingled. There is a possibility that a 14mm tibial bearing is packaged in a box labeled as 12 mm tibial bearing and vice versa. This may lead to extension of surgery to find another implant. 48 2020-04-07
Biomet, Inc. 510(k) number 2018-05-11 Class II Under Investigation by firm The label master file was errantly set up as a 63/37mm instead of a 63/67mm. There is no 63/37 size offered, and the product is laser marked with the correct size. 169 2019-11-21
Biomet, Inc. 510(k) number 2017-10-03 Class II Error in labeling The affected products are labeled as a 62.5mm LEFT Femur; however, the contents are a Vanguard 70mm RIGHT Femur. 8 2018-08-23
Biomet, Inc. 510(k) number 2016-08-08 Class II Process control The drill bit used to drill the hex pre-drilled hole in the screw head of the Tibial Augment Bolts included in the Vanguard 360 Revision Knee System was larger than allowable per the process specification. As a result, the hex geometry can 454 2017-06-05
Biomet, Inc. 510(k) number 2014-07-01 Class II Process change control The Vanguard 360 Femoral Boss Reamers were manufactured oversized to the print. The instrument may not fit into the mating component. 461 2015-10-30

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