Genesis

Genisis Tibia Poly Onlay Extra Small Right Medial/Left Lateral 11MM

Registry build 21.09.26
6manufacturers in China registered for this device type
118catalogue 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 Genesis
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) K230653
Record published 2015-08-25
Record revised 2025-11-18 (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 2017-05-22

Catalogue Numbers

Catalogue numbers for Genesis
Catalogue number Size Status
71243210 In distribution
71243310 In distribution
71243421 In distribution
71248341 In distribution
71243422 In distribution
71248331 In distribution
71243320 In distribution
71243118 In distribution
71243620 In distribution
71243319 In distribution
725004 In distribution
727305 In distribution
71243618 In distribution
71243622 In distribution
726100 In distribution
726202 In distribution
71248342 In distribution
726304 In distribution
71243418 In distribution
71248230 In distribution
71248232 In distribution
71243420 In distribution
725003 In distribution
725006 In distribution
71243411 In distribution
71243510 In distribution
71243518 In distribution
71248338 In distribution
71243108 In distribution
71243311 In distribution
71243309 In distribution
71243121 In distribution
71243215 In distribution
71248229 In distribution
725557 In distribution
71243120 In distribution
71248318 In distribution
727100 In distribution
71242515 In distribution
71248231 In distribution
71243318 In distribution
727202 In distribution
71243212 In distribution
71243412 In distribution
71243122 In distribution
71243619 In distribution
71243110 In distribution
71243611 In distribution
71243218 In distribution
725001 In distribution
71243308 In distribution
71248340 In distribution
71243520 In distribution
71243612 In distribution
726203 In distribution
71243322 In distribution
71244509 In distribution
71243512 In distribution
71248339 In distribution
71248332 In distribution
71243208 In distribution
71243519 In distribution
71243608 In distribution
726101 In distribution
71243522 In distribution
725005 In distribution
71248228 In distribution
71243109 In distribution
71243211 In distribution
71243221 In distribution
71243610 In distribution
71248329 In distribution
71243521 In distribution
71243312 In distribution
71243125 In distribution
726305 In distribution
727101 In distribution
71243111 In distribution
71243408 In distribution
71243409 In distribution
71243220 In distribution
114861 In distribution
727304 In distribution
71243112 In distribution
71243509 In distribution
71243209 In distribution
71243410 In distribution
71248330 In distribution
71243609 In distribution
725002 In distribution
727203 In distribution
71243508 In distribution
71243015 In distribution
71243511 In distribution
71243119 In distribution
71243222 In distribution
71243621 In distribution
71243009 In distribution
71243115 In distribution
71245007 In distribution
71243321 In distribution
71242410 Withdrawn
71242412 Withdrawn
71932125 Withdrawn
71932124 Withdrawn
71242610 Withdrawn
71932323 Withdrawn
71242510 Withdrawn
71242509 Withdrawn
71242409 Withdrawn
71932123 Withdrawn
71928021 Withdrawn
71242609 Withdrawn
71932122 Withdrawn
71242615 Withdrawn
71242415 Withdrawn
71242612 Withdrawn
71242512 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
Journey II Smith & Nephew, Inc. 119

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 Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of Genesis
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Smith & Nephew, Inc. 510(k) number 2004-06-21 Not classified Other The firm received confirmed reports of Genesis Uni Articular Inserts not locking into tibial base plates intraoperatively. 11,339 units were distributed 2006-02-15

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