PRO

Suprapectineal Flex Plate 12-hole, right

Registry build 21.09.26
22manufacturers in China registered for this device type
49catalogue numbers in this listing
25510(k) clearances naming this product code
1recall

Who Else Makes It

Concentrated in Jiangsu (10), Shanghai (4), Zhejiang (3). 12 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HRS
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
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
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Suzhou Kangli Orthopaedics Instrument Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 11
Kingj Medical Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 7
Hangzhou Sino-MIM Technology Co., Ltd. Hangzhou Zhejiang Contract manufacturer 6
Suzhou AND Science & Technology Development Corp. Zhangjiagang Jiangsu Contract manufacturer 5
Beijing AK Medical Co., Ltd. Changping District Beijing Contract manufacturer 3

Showing 12 of 22. All 22 manufacturers in China registered for Plate, Fixation, Bone

Record

Regulatory record for PRO
Listed by Stryker GmbH, Switzerland
FDA product code HRS
Device type Plate, Fixation, Bone
Device class Class 2
Regulation 21 CFR 888.3030
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer
Record published 2015-09-24
Record revised 2025-11-20 (version 12)

Specifications

Specifications
MRI safety MR Conditional
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for PRO
Catalogue number Size Status
425911 In distribution
425941S In distribution
425900 In distribution
425974S Side: LEFT In distribution
425961S In distribution
425982 Side: LEFT In distribution
940070 In distribution
425941 In distribution
425942S Side: LEFT In distribution
425901S In distribution
425973 Side: RIGHT In distribution
425981 Side: RIGHT In distribution
425973S Side: RIGHT In distribution
425962 In distribution
425932 In distribution
425906S In distribution
425905S In distribution
425986 In distribution
425971S Side: RIGHT In distribution
425972S Side: LEFT In distribution
425942 In distribution
425922S In distribution
425951 In distribution
425985S In distribution
425900S In distribution
940076 In distribution
425972 In distribution
425906 In distribution
425961 In distribution
425963S Side: RIGHT In distribution
425901 In distribution
425922 In distribution
425911S In distribution
425912 In distribution
425952S Side: LEFT In distribution
425964 In distribution
940075 In distribution
425962S Side: LEFT In distribution
425905 In distribution
425974 In distribution
425985 In distribution
425982S Side: LEFT In distribution
425952 In distribution
425981S Side: RIGHT In distribution
425971 In distribution
425964S Side: LEFT In distribution
425986S In distribution
425951S Side: RIGHT In distribution
425963 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Pectus System Biomet Microfixation 4,662
Arthrex® Arthrex, Inc. 3,031
Evos Smith & Nephew, Inc. 2,235
Peri-Loc Smith & Nephew, Inc. 2,196
OsteoMed Osteomed 1,961
VariAx Stryker GmbH 1,934
Aptus Medartis Inc. 1,688
TC-100 Smith & Nephew, Inc. 1,639
Plate, Fixation, Bone Synthes Gmbh 1,613
Anthem Globus Medical, Inc. 1,551
Acumed Acumed LLC 1,360
Signex Osteonic Co., Ltd. 1,310

Showing 12 of 3,530. All products under Plate, Fixation, Bone

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K242445 2024-10-06
K233919 2024-03-25
K231257 2023-08-18
K231262 2023-08-18
K222381 2023-04-27
K223772 2023-04-07
K221346 2022-07-08
K212581 2022-01-19
K200398 2020-06-05
K192675 2019-11-22
K191412 2019-08-23
K183172 2019-03-05
K181091 2018-10-11
K172148 2018-03-19
K172350 2017-12-15
K170727 2017-06-22
K170771 2017-05-08
K162841 2017-02-21
K162439 2017-02-03
K153379 2016-05-26
K151769 2015-10-27
K151879 2015-08-06
K113109 2011-12-23
K112926 2011-12-19
K110476 2011-03-18

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
2019-12-05 Class II Under Investigation by firm Instrument can break at the level of the thread when being exposed to high forces during nail implantation or removal which can lead to complications during nail insertion and removal. 433 (289 units U.S. / 144 units OUS) 2020-10-09

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