Vanguard XP® Instrumentation

127 catalogue numbers from 32-700184, 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
127catalogue 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 XP® Instrumentation
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) K122160
Record published 2021-03-24
Record revised 2025-05-30 (version 7)

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

Catalogue Numbers

Catalogue numbers for Vanguard XP® Instrumentation
Catalogue number Size Status
32-700184 10 mm X 59 mm In distribution
32-700242 12 mm X 69/71 mm In distribution
32-700334 13 mm X 87 mm In distribution
32-700150 11 mm X 59 mm In distribution
32-700375 In distribution
32-700016 65MM RIGHT In distribution
32-700091 16MM X 63 / 65 / 67MM In distribution
32-700111 14MM X 87/91MM In distribution
32-700409 57.5 mm In distribution
32-700299 13 mm X 65/67 mm In distribution
32-700153 14 mm X 59 mm In distribution
32-700167 14 mm X 69/71/73/75 mm In distribution
32-700410 60MM, LEFT In distribution
32-700308 16MM X 69/71MM In distribution
32-700248 11MM X 73/75MM In distribution
32-700060 73MM TIBIAL TRAY TRIAL In distribution
32-700306 13 mm X 69/71 mm In distribution
32-700322 16MM X 79MM In distribution
32-700196 16MM X 63 / 65 / /67MM In distribution
32-700307 14 mm X 69/71 mm In distribution
32-700420 Size 59 mm In distribution
32-700119 16 mm 59 mm In distribution
32-700179 12 mm X 87/91 mm In distribution
32-700273 16MM X 87MM In distribution
32-700107 10MM X 87/91MM In distribution
32-700057 67 mm In distribution
32-700092 9 mm X 69/71/73/75 mm In distribution
32-700406 80 mm In distribution
32-700099 9MM X 79/83MM In distribution
32-700267 9MM X 87MM In distribution
32-700104 14 mm X 79/83 mm In distribution
32-700297 11 mm X 65/67 mm In distribution
32-700285 13 mm X 59 mm In distribution
32-700330 9 mm X 87 mm In distribution
32-700331 10MM X 87MM In distribution
32-700149 10 mm X 59 mm In distribution
32-700060 73 mm In distribution
32-700141 9MM X 87/91MM In distribution
32-700024 57.5MM LEFT In distribution
32-700409 57.5MM, LEFT In distribution
32-700205 10MM X 79/83MM In distribution
32-700131 13MM X69/71/73/75MM In distribution
32-700152 13 mm X 59 mm In distribution
32-700207 12MM X 79/83MM In distribution
32-700260 9MM X 83MM In distribution
32-700240 10MM X 69/71MM In distribution
32-700026 62.5MM LEFT In distribution
32-700192 11 mm X 63/65/67 mm In distribution
32-700251 14MM X 73/75MM In distribution
32-700221 12 mm X 59 mm In distribution
32-700289 10MM X 63MM In distribution
32-700020 75MM RIGHT In distribution
32-700320 13 mm X 79 mm In distribution
32-700168 16 mm X 69/71/73/75 mm In distribution
32-700232 9MM X 65/67MM In distribution
32-700294 16 mm X 63 mm In distribution
32-700286 14 mm X 59 mm In distribution
32-700310 10MM X 73/75MM In distribution
32-700164 11 mm X 69/71/73/75 mm In distribution
32-700127 9MM X 69/71/73/75MM In distribution
32-700388 SIZES 87-91 In distribution
32-700059 71 mm In distribution
32-700136 11 mm X 79/83 mm In distribution
32-700238 16 mm X 65/67 mm In distribution
32-700156 10 mm X 63/65/67 mm In distribution
32-700408 55MM, LEFT In distribution
32-700298 12 mm X 65/67 mm In distribution
32-700241 11MM X 69/71MM In distribution
32-700143 11MM X 87/91MM In distribution
32-700103 13MM X 79/83MM In distribution
32-700210 16 mm X 79/83 mm In distribution
32-700214 12 mm X 87/91 mm In distribution
32-700366 In distribution
32-700249 12 mm X 73/75 mm In distribution
32-700326 12 mm X 83 mm In distribution
32-700202 14 mm X 69/71/73/75 mm In distribution
32-700125 14MM X 63/65/67MM In distribution
32-700271 13MM X 87MM In distribution
32-700314 14MM X 73/75MM In distribution
32-700323 9MM X 83MM In distribution
32-700175 16MM X 79 / 83MM In distribution
32-700106 9MM X 87/91MM In distribution
32-700104 14MM X 79/83MM In distribution
32-700326 12MM X 83MM In distribution
32-700414 70 mm In distribution
32-700135 10 mm X 79/83 mm In distribution
32-700085 9 mm X 63/65/67 mm In distribution
32-700070 69-83 mm In distribution
32-700216 14MM X 87/91MM In distribution
32-700405 77.5 mm In distribution
32-700162 9 mm X 69/71/73/75 mm In distribution
32-700295 9 mm X 65/67 mm In distribution
32-700214 12MM X 87/91MM In distribution
32-700258 14 mm X 79 mm In distribution
32-700384 SIZES 63-83 In distribution
32-700086 10 mm X 63/65/67 mm In distribution
32-700237 14MM X 65/67MM In distribution
32-700252 16 mm X 73/75 mm In distribution
32-700413 67.5MM, LEFT In distribution
32-700019 72.5MM RIGHT In distribution
32-700066 59-67 mm In distribution
32-700194 13 mm X 63/65/67 mm In distribution
32-700266 16 mm X 83 mm In distribution
32-700118 14 mm 59 mm In distribution
32-700303 10MM X 69/71MM In distribution
32-700087 11 mm X 63/65/67 mm In distribution
32-700407 52.5MM, LEFT In distribution
32-700263 12MM X 83MM In distribution
32-700179 12MM X 87/91MM In distribution
32-700126 16 mm X 63/65/67 mm In distribution
32-700325 11MM X 83MM In distribution
32-700298 12MM X 65/67MM In distribution
32-700288 9 mm X 63 mm In distribution
32-700100 10 mm X 79/83 mm In distribution
32-700203 16MM X 69 / 71 / 73 / 75MM In distribution
32-700209 14 mm X 79/83 mm In distribution
32-700401 67.5MM, RIGHT In distribution
32-700399 62.5 mm In distribution
32-700103 13 mm X 79/83 mm In distribution
32-700217 16MM X 87/91MM In distribution
32-700306 13MM X 69/71MM In distribution
32-700339 11 mm X 91 mm In distribution
32-700068 87 – 91MM In distribution
32-700250 13MM X 73/75MM In distribution
32-700261 10MM X 83MM In distribution
32-700058 69 mm In distribution
32-700317 10MM X 79MM 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

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

Recalls naming the identifiers of Vanguard XP® Instrumentation
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Biomet, Inc. 510(k) number 2019-08-15 Class II Manufacturing material removal The locking bar not fully engaging 45 units 2021-04-16
Biomet, Inc. 510(k) number 2019-08-15 Class II Manufacturing material removal The locking bar not fully engaging 2 units 2021-04-16
Biomet, Inc. 510(k) number 2019-08-15 Class II Manufacturing material removal The locking bar not fully engaging 8 units 2021-04-16
Biomet, Inc. 510(k) number 2019-08-15 Class II Manufacturing material removal The locking bar not fully engaging 43 units 2021-04-16
Biomet, Inc. 510(k) number 2019-08-15 Class II Manufacturing material removal The locking bar not fully engaging 74 units 2021-04-16
Biomet, Inc. 510(k) number 2019-08-15 Class II Manufacturing material removal The locking bar not fully engaging 123 units 2021-04-16
Biomet, Inc. 510(k) number 2019-08-15 Class II Manufacturing material removal The locking bar not fully engaging 2021-04-16
Biomet, Inc. 510(k) number 2019-08-15 Class II Manufacturing material removal The locking bar not fully engaging 84 units 2021-04-16
Biomet, Inc. 510(k) number 2019-08-15 Class II Manufacturing material removal The locking bar not fully engaging 110 units 2021-04-16
Biomet, Inc. 510(k) number 2019-08-15 Class II Manufacturing material removal The locking bar not fully engaging 99 units 2021-04-16
Biomet, Inc. 510(k) number 2019-08-15 Class II Manufacturing material removal The locking bar not fully engaging 49 units 2021-04-16
Biomet, Inc. 510(k) number 2019-08-15 Class II Manufacturing material removal The locking bar not fully engaging 2021-04-16
Biomet, Inc. 510(k) number 2016-02-05 Class II Device Design The anterior/posterior (AP) dimension may be oversized by 0.016.
If the femoral component does not fit as tightly as intended, bony ingrowth may not occur causing loosening of the femoral component. A revision surgery may be necessary.
890 2017-03-28

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