VLP Foot

VLP 2.7MM Percutaneous Calcaneus Plate Extra-Large Right 68MM Sterile

Registry build 21.09.26
22manufacturers in China registered for this device type
323catalogue numbers in this listing
37510(k) clearances naming this product code
15recalls on this code

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 VLP Foot
Listed by Smith & Nephew, Inc., United States
FDA product code HRS
Device type Plate, Fixation, Bone
Device class Class 2
Regulation 21 CFR 888.3030
Establishment Contract manufacturer, Remanufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K090675
Record published 2015-08-29
Record revised 2026-04-01 (version 10)

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
Packaging Box of 6
Distribution end date 2022-03-17
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for VLP Foot
Catalogue number Size Status
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72824027S Size: 3.5MM ONE-THIRD 7 Hole In distribution
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Showing 250 of 300 catalogue numbers.

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
K241666 2025-02-19
K240487 2024-09-03
K223762 2023-05-30
K213123 2022-10-18
K210837 2021-06-29
K203405 2021-01-27
K201918 2020-11-16
K201527 2020-07-22
K190253 2019-03-11
K181533 2018-08-09
K173293 2018-01-08
K172262 2017-08-23
K170457 2017-06-14
K170887 2017-04-24
K163086 2016-12-21
K162078 2016-11-18
K161665 2016-11-15
K152976 2015-11-12
K143050 2014-12-18
K140814 2014-05-07
K132886 2014-02-04
K132296 2014-01-07
K123055 2013-01-25
K120667 2012-04-04
K112406 2011-11-14
K110670 2011-07-12
K092015 2009-07-30
K090675 2009-06-04
K083032 2009-01-07
K081106 2008-06-18
K072818 2007-11-19
K071563 2007-08-08
K062216 2006-09-15
K061352 2006-06-08
K051735 2005-07-19
K033669 2003-12-10
K993106 1999-12-09

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 VLP Foot
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Smith & Nephew, Inc. 510(k) number 2017-03-09 Class II Labeling Change Control The expiration dates on the labeling are incorrect, the actual expiration dates are before the date on the labeling. 1 unit 2019-08-21

Recalls

13 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
2022-01-04 Class II Process control The affected screwdrivers are out of specification and may not mate with the Surfix Alpha Lock screw 8 units (US)
2021-11-01 Class II Under Investigation by firm Testing vendor notified Smith & Nephew that previous MRI scanning conditions provided in Exponents reports were erroneous. Erroneous data from the reports was incorporated in the released IFU
81110294 EVOS Large Fragment Plating System.
35 units 2026-06-15
2021-11-01 Class II Under Investigation by firm Testing vendor notified Smith & Nephew that previous MRI scanning conditions provided in Exponents reports were erroneous. Erroneous data from the reports was incorporated in the released IFU
81110294 EVOS Large Fragment Plating System.
38 units 2026-06-15
2021-11-01 Class II Under Investigation by firm Testing vendor notified Smith & Nephew that previous MRI scanning conditions provided in Exponents reports were erroneous. Erroneous data from the reports was incorporated in the released IFU
81110294 EVOS Large Fragment Plating System.
35 units 2026-06-15
2021-11-01 Class II Under Investigation by firm Testing vendor notified Smith & Nephew that previous MRI scanning conditions provided in Exponents reports were erroneous. Erroneous data from the reports was incorporated in the released IFU
81110294 EVOS Large Fragment Plating System.
41 units 2026-06-15
2021-10-25 Class II Error in labeling The labels on the packages of screws were switched. 224 units
2020-08-24 Class II Error in labeling Multiple or incorrect expiration dates were provided on the affected designation labels. 71 units 2022-07-11
2017-12-11 Class II Mixed-up of materials/components Devices, incorrectly labeled as a VLP MINI-MOD 2.0MM STRAIGHT PLATE 8 HOLE, contained a VLP MINI-MOD 2.0MM STOUT PLATE 8 HOLE and vice versa 2 units 2018-06-22
2017-12-11 Class II Mixed-up of materials/components Devices, incorrectly labeled as a VLP MINI-MOD 2.0MM STRAIGHT PLATE 8 HOLE, contained a VLP MINI-MOD 2.0MM STOUT PLATE 8 HOLE and vice versa 2 units 2018-06-22
2017-11-29 Class II Employee error One lot of EVOS 2.4MM Flex Plate 6 Hole packaging contained templates. 12 2020-09-01
2017-03-22 Class II Mixed-up of materials/components This lot of left plates were laser etched and packaged as right plates. 12 units 2022-06-03
2015-10-20 Class II Employee error The devices were packaged and laser marked anatomically incorrect. The Left plates were laser marked and packaged as Right plates and the Right plates were laser marked and packaged as Left plates. 9 units 2016-09-21
2015-10-20 Class II Employee error The devices were packaged and laser marked anatomically incorrect. The Left plates were laser marked and packaged as Right plates and the Right plates were laser marked and packaged as Left plates. 9 units 2016-09-21
2010-07-20 Not classified Packaging Inner packaging of sterile product was not sealed. Lack of sterility assurance. 10 units 2011-11-17

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