Journey II

Journey II UNI Baseplate Trial Size 1 LM/RL

Registry build 21.09.26
6manufacturers in China registered for this device type
119catalogue numbers in this listing
13510(k) clearances naming this product code
40recalls on this code

Who Else Makes It

Concentrated in Zhejiang (2), Jiangsu (2), Shanghai (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 HSX
Manufacturer City Province Registered as Device types
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
Turnxon Precision Co., Ltd. Dongguan Guangdong Contract manufacturer 17
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74

Record

Regulatory record for Journey II
Listed by Smith & Nephew, Inc., United States
FDA product code HSX
Device type Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer
Device class Class 2
Regulation 21 CFR 888.3520
Establishment Contract manufacturer, Remanufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K152315
Record published 2015-11-25
Record revised 2023-09-07 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Storage Special storage condition: : –
Distribution end date 2022-03-17

Catalogue Numbers

Catalogue numbers for Journey II
Catalogue number Size Status
71935088 In distribution
71935108 In distribution
E0017507-8 In distribution
71935109 In distribution
71935162 In distribution
71935212 In distribution
E0017507-2 In distribution
71935099 In distribution
71935220 In distribution
71935101 In distribution
E0017507-6 In distribution
71935094 In distribution
E0016324-1 In distribution
71935103 In distribution
71935166 In distribution
E0017507-1 In distribution
71935227 In distribution
E0017499-1 In distribution
E0017499-8 In distribution
71935226 In distribution
E0018019-3 In distribution
71935107 In distribution
71935155 In distribution
71935148 In distribution
71935219 In distribution
71935228 In distribution
71935218 In distribution
71935217 In distribution
E0015788-1 In distribution
71935160 In distribution
71935176 In distribution
71935208 In distribution
E0017237-2 In distribution
71935204 In distribution
E0016204-1 In distribution
71935095 In distribution
71935090 In distribution
71935178 In distribution
71935167 In distribution
71935214 In distribution
71935164 In distribution
71935098 In distribution
E0017499-7 In distribution
71935168 In distribution
E0015612-4 In distribution
71935193 In distribution
71935224 In distribution
71935213 In distribution
71935147 In distribution
71935149 In distribution
71935183 In distribution
71935207 In distribution
71935104 In distribution
71935096 In distribution
71935092 In distribution
71935158 In distribution
71935091 In distribution
71935175 In distribution
E0015810-1 In distribution
71935205 In distribution
71935106 In distribution
E0015997-3 In distribution
71935221 In distribution
E0017499-6 In distribution
71935156 In distribution
71935209 In distribution
71935222 In distribution
71935093 In distribution
E0016231-6 In distribution
E0015907-1 In distribution
71935225 In distribution
E0016234-6 In distribution
E0017499-3 In distribution
71935152 In distribution
E0017507-3 In distribution
71935157 In distribution
71935111 In distribution
71935163 In distribution
E0016054-5 In distribution
71935198 In distribution
71935216 In distribution
71935206 In distribution
71935201 In distribution
71935200 In distribution
71935215 In distribution
71935159 In distribution
71935153 In distribution
71935210 In distribution
E0015996-3 In distribution
71935211 In distribution
71935161 In distribution
E0017507-5 In distribution
71935223 In distribution
71935102 In distribution
71935100 In distribution
71935173 In distribution
71935110 In distribution
E0017507-7 In distribution
71935197 In distribution
71935199 In distribution
71935194 In distribution
E0016619-1 In distribution
71935105 In distribution
71935097 In distribution
71935203 In distribution
71935151 In distribution
71935195 In distribution
E0017499-5 In distribution
E0017507-4 In distribution
71935202 In distribution
71935089 In distribution
71935177 In distribution
71935165 In distribution
E0017499-2 In distribution
71935174 In distribution
E0017499-4 In distribution
E0016054-6 In distribution
71935196 In distribution
E0014975-3 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Journey Smith & Nephew, Inc. 517
Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer Ortho Development Corp. 303
BKS® Uni Ortho Development Corp. 240
LinkSymphoKnee Waldemar Link GmbH & Co. KG 210
Moto Partial Knee System Medacta International SA 205
Arthrex® Arthrex, Inc. 199
Stride Smith & Nephew, Inc. 190
Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer Zimmer, Inc. 175
ZUK Smith & Nephew, Inc. 161
Tahoe Uni Knee System Shalby Advanced Technologies, Inc. 134
Moto Partial Knee System – Medial Medacta International SA 132
Genesis Smith & Nephew, Inc. 118

Showing 12 of 171. All products under Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K242711 2024-10-30
K211512 2021-09-16
K191211 2019-07-25
K190085 2019-02-11
K160738 2016-06-15
K152315 2015-10-28
K113038 2012-01-05
K102069 2010-10-05
K100197 2010-02-19
K081351 2008-07-24
K073175 2007-12-20
K061779 2006-08-04
K061011 2006-07-11

Recalls

7 of these are 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
2023-05-02 Class II Under Investigation by firm Recent complaint data indicates that the revision rate may be trending higher than corresponding similar devices in global joint replacement registries. The data identifies a potential signal that the performance is an outlier versus the st 1596 units
2023-05-02 Class II Under Investigation by firm Recent complaint data indicates that the revision rate may be trending higher than corresponding similar devices in global joint replacement registries. The data identifies a potential signal that the performance is an outlier versus the st 7531 units
2023-05-02 Class II Under Investigation by firm Recent complaint data indicates that the revision rate may be trending higher than corresponding similar
devices in global joint replacement registries. The data identifies a potential signal that the performance is an outlier versus the st
1994 units
2023-05-02 Class II Under Investigation by firm Recent complaint data indicates that the revision rate may be trending higher than corresponding similar devices in global joint replacement registries. The data identifies a potential signal that the performance is an outlier versus the st 2146 units
2023-03-27 Class II Under Investigation by firm A mispack occurred during the manufacturing process, resulting in the box incorrectly containing JOURNEY II UNI Tibia Insert Medical Size 1-2 12MM instead of the JOURNEY II UNI Tibia Insert Medial Size 7-8 8MM. 12 units
2020-01-28 Class II Process design The spike rail was manufactured with an oversized thru-hole which could potentially cause the dowel pin to fall out and the device to disassemble. 195 units 2023-12-11
2020-01-28 Class II Process design The spike rail was manufactured with an oversized thru-hole which could potentially cause the dowel pin to fall out and the device to disassemble. 200 units 2023-12-11
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 58 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 859 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 904 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 941 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 1421 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 353 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 1150 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 71 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 1004 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 704 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 56 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 628 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 849 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 817 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 60 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 57 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 960 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 838 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 379 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 863 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 895 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 734 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 89 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 1064 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 813 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 721 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 97 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 1283 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 69 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 952 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 713 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 1324 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 1015 units 2011-03-25

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