VA-LCP

2.7MM TI VA-LCP Lateral Distal Fibula PLATE/13 Holes/LT-Ster

Registry build 21.09.26
22manufacturers in China registered for this device type
539catalogue numbers in this listing
9510(k) clearances naming this product code
8recalls 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 VA-LCP
Listed by Synthes Gmbh, Switzerland
FDA product code HRS
Device type Plate, Fixation, Bone
Device class Class 2
Regulation 21 CFR 888.3030
Establishment Specification developer, Manufacturer, Exporter
510(k) K092556
Record published 2015-09-14
Record revised 2025-11-20 (version 13)

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
Supplied as a kit Yes
Label carries lot or batch number, expiry date
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for VA-LCP
Catalogue number Size Status
04.111.530 In distribution
02.118.207 In distribution
04.107.304 In distribution
02.115.530 In distribution
02.211.231S In distribution
04.117.408S In distribution
04.107.510 In distribution
02.115.630S In distribution
02.111.690S In distribution
02.127.240 In distribution
02.111.681S In distribution
04.111.551 In distribution
04.118.415S In distribution
04.112.049S In distribution
04.117.104 In distribution
02.118.009 In distribution
04.115.451 In distribution
04.111.651S In distribution
02.111.680S In distribution
04.117.402S In distribution
03.127.010 In distribution
02.211.230S In distribution
04.117.013S In distribution
02.124.419S In distribution
02.111.620S In distribution
02.118.206 In distribution
02.115.350S In distribution
04.118.404S In distribution
02.118.215 In distribution
02.115.150 In distribution
02.117.103 In distribution
02.211.260S In distribution
02.115.150S In distribution
04.111.741 In distribution
04.111.640S In distribution
04.107.506 In distribution
04.111.641 In distribution
04.111.531S In distribution
02.107.510 In distribution
02.111.750S In distribution
02.115.230S In distribution
02.111.651 In distribution
04.117.311S In distribution
02.117.203S In distribution
02.211.241S In distribution
04.115.630S In distribution
02.115.231 In distribution
04.111.631 In distribution
04.117.207 In distribution
04.117.009 In distribution
04.117.207S In distribution
02.107.304 In distribution
02.115.151S In distribution
02.115.251S In distribution
04.115.151S In distribution
04.117.203 In distribution
04.117.608S In distribution
02.111.770S In distribution
04.115.640 In distribution
02.118.409S In distribution
04.211.254 In distribution
02.115.330S In distribution
04.115.530S In distribution
04.111.670S In distribution
02.111.571S In distribution
02.117.901S In distribution
02.111.641S In distribution
04.111.541S In distribution
04.117.107 In distribution
02.118.400S In distribution
04.117.610S In distribution
02.111.731 In distribution
04.111.630KS In distribution
02.115.350 In distribution
04.118.405 In distribution
02.111.640S In distribution
04.115.641 In distribution
02.211.243S In distribution
02.112.048S In distribution
02.118.212S In distribution
02.124.418 In distribution
04.111.740 In distribution
02.117.902S In distribution
04.118.406S In distribution
04.111.750 In distribution
04.107.412S In distribution
02.118.411S In distribution
02.211.238S In distribution
02.211.251 In distribution
04.117.011S In distribution
02.111.650 In distribution
04.111.730 In distribution
04.211.234 In distribution
04.117.909S In distribution
04.111.621 In distribution
02.211.247S In distribution
04.115.131S In distribution
02.110.204 In distribution
02.107.206S In distribution
02.124.415 In distribution
02.111.621S In distribution
02.211.237S In distribution
04.111.540S In distribution
02.118.415 In distribution
02.111.740S In distribution
02.115.231S In distribution
02.111.741S In distribution
04.111.721 In distribution
02.115.330 In distribution
02.211.421S In distribution
02.118.002 In distribution
02.111.521S In distribution
04.115.230 In distribution
02.115.751S In distribution
02.111.520S In distribution
02.118.405S In distribution
02.118.401 In distribution
04.111.650S In distribution
04.115.631S In distribution
02.117.313S In distribution
02.115.850 In distribution
03.118.102 In distribution
02.118.302S In distribution
02.117.204 In distribution
02.211.258S In distribution
04.111.741S In distribution
04.211.231 In distribution
04.117.510S In distribution
04.117.113S In distribution
04.211.261 In distribution
02.115.250 In distribution
04.111.740S In distribution
02.211.236S In distribution
02.211.418 In distribution
02.115.631 In distribution
04.118.409 In distribution
02.127.211S In distribution
04.115.450S In distribution
02.117.013S In distribution
04.117.807S In distribution
04.115.751 In distribution
02.118.404 In distribution
04.115.430 In distribution
02.110.207 In distribution
04.117.107S In distribution
04.117.109S In distribution
02.211.254S In distribution
02.118.005 In distribution
02.110.205 In distribution
02.107.412S In distribution
02.124.418S In distribution
04.111.750S In distribution
02.115.631S In distribution
04.117.213S In distribution
02.110.201 In distribution
04.117.007 In distribution
02.127.340 In distribution
02.117.702 In distribution
04.117.404S In distribution
04.118.406 In distribution
02.117.502S In distribution
03.231.006 In distribution
02.117.905 In distribution
02.211.232 In distribution
02.118.105S In distribution
04.118.402 In distribution
02.127.261 In distribution
04.117.911S In distribution
02.111.730 In distribution
02.111.720S In distribution
02.118.005S In distribution
04.111.520S In distribution
02.117.203 In distribution
04.107.306S In distribution
02.111.650S In distribution
02.115.640 In distribution
04.111.570S In distribution
02.115.431 In distribution
02.111.540 In distribution
02.127.251 In distribution
02.117.604S In distribution
04.115.130S In distribution
04.117.601S In distribution
02.110.202 In distribution
02.115.640S In distribution
04.107.102S In distribution
04.117.401S In distribution
04.111.751S In distribution
02.117.209 In distribution
02.118.013 In distribution
02.111.631S In distribution
02.117.011S In distribution
02.117.801S In distribution
04.111.551S In distribution
02.115.751 In distribution
02.117.009S In distribution
04.118.409S In distribution
02.115.641S In distribution
04.117.905S In distribution
02.127.331 In distribution
02.117.501 In distribution
02.118.007 In distribution
02.118.205 In distribution
02.111.631KS In distribution
02.111.771S In distribution
04.111.631S In distribution
04.111.571S In distribution
04.211.251 In distribution
02.115.130S In distribution
04.107.202S In distribution
02.111.531 In distribution
02.118.217S In distribution
02.117.704S In distribution
04.115.431S In distribution
02.118.014 In distribution
03.118.101 In distribution
04.115.540S In distribution
02.117.408S In distribution
04.115.641S In distribution
04.211.238 In distribution
02.111.541 In distribution
02.211.419 In distribution
04.118.412 In distribution
02.117.303 In distribution
04.111.530S In distribution
02.117.007 In distribution
04.211.250S In distribution
02.117.107S In distribution
04.115.131 In distribution
02.111.720 In distribution
03.231.001 In distribution
02.127.360 In distribution
02.211.238 In distribution
02.117.209S In distribution
02.111.751 In distribution
04.115.451S In distribution
02.115.451S In distribution
02.111.570S In distribution
04.115.431 In distribution
04.110.207 In distribution
04.110.201 In distribution
02.111.741 In distribution
02.211.259S In distribution
02.118.407S In distribution
04.111.731S In distribution
04.211.256S In distribution
02.117.207S In distribution
04.117.805S In distribution
02.127.330S In distribution
04.115.150S In distribution

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
K254093 2026-03-10
K260069 2026-03-09
K254054 2026-03-02
K233994 2024-07-26
K233967 2024-05-09
K112689 2011-10-26
K093772 2010-03-29
K020602 2002-05-20
K982732 1998-10-08

Recalls Naming This Product

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

Recalls naming the identifiers of VA-LCP
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Synthes (USA) Products LLC 510(k) number 2016-06-28 Class II Nonconforming Material/Component It was reported that the specified lots of the 2.4mm Titanium Locking Screw Self-Tapping with Stardrive Recess 12mm can break between the head and the shaft. This resulted from the neck feature being too close to the StarDrive feature leav 41 units 2017-02-02
Synthes (USA) Products LLC 510(k) number 2015-11-02 Class II Process control It was discovered that the above part number and lot of 2.4mm Locking Screws may contain the incorrect package insert (GP2613, VA-LCP Distal Radius System). The correct package insert for the above part is GP2615 (Modular Mini Fragment LCP 229 2016-07-15
Synthes (USA) Products LLC 510(k) number 2015-09-28 Class II Labeling mix-ups The 2.7MM/3.5MM VA-LCP Humerus Plates were found to be labeled incorrectly. Part number 02.117.410S was incorrectly etched with part number 02.117.610S 36 2016-12-06
Synthes Gmbh 510(k) number 2014-02-05 Class II Employee error Labeling correction: The package insert in one 5.0mm Variable Locking Screw package was a GP0006 (Anterior Cervical Vertebrae Plate System) insert, which should have been a GP2848 (4.5mm VA-LCP Curved Condylar Plate System insert). 45 2015-08-31
Synthes USA (HQ), Inc. 510(k) number 2013-07-30 Class II Process control The possibility exists that 2.4 mm VA-LCP 2 column distal radius plates from a specific lot are etched with “R” for right plate when they should be etched with “L” for left plate. 11 2015-05-21
Synthes (USA) Products LLC 510(k) number 2013-05-31 Class II Device Design The firm is initiating a Field Safety Correction for the labeling of the 2.4mm VA-LCP Two Column Volar Distal Radius Plate and 1.2 Nm Torque Limiting Attachment. The US Technique guide lists 1.2Nm TLA as an option for use with the 2.4mm Var 119, 891 2015-09-21
Synthes USA (HQ), Inc. 510(k) number 2013-05-29 Class II Employee error A plate was inadvertently released to a sales consultant that was restricted for sale. 1 2015-05-21
Synthes USA (HQ), Inc. 510(k) number 2013-01-11 Class II Labeling mix-ups It was discovered that one of the VA-LCP Dorsal Distal Radius Plates was incorrectly etched as Part Number 02.115.431 (110 degree) instead of the correct Part Number 02.115.231 (90 degree). 4 2015-08-31
Synthes Gmbh 510(k) number 2006-12-05 Not classified Other Hole is malformed, leading to reduced construct strength. 11 units 2007-02-13

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
2019-12-16 Class II Under Investigation by firm There is a possibility that the inner cap could open when the outer cap is removed or the entire inner tube remains in the outer tube. In both instances this could prevent the screw from being removed and used causing a surgical delay. The 25 total 2020-06-08
2019-12-16 Class II Under Investigation by firm There is a possibility that the inner cap could open when the outer cap is removed or the entire inner tube remains in the outer tube. In both instances this could prevent the screw from being removed and used causing a surgical delay. The 25 total 2020-06-08
2019-12-16 Class II Under Investigation by firm There is a possibility that the inner cap could open when the outer cap is removed or the entire inner tube remains in the outer tube. In both instances this could prevent the screw from being removed and used causing a surgical delay. The 25 total 2020-06-08
2019-12-16 Class II Under Investigation by firm There is a possibility that the inner cap could open when the outer cap is removed or the entire inner tube remains in the outer tube. In both instances this could prevent the screw from being removed and used causing a surgical delay. The 25 total 2020-06-08
2019-12-16 Class II Under Investigation by firm There is a possibility that the inner cap could open when the outer cap is removed or the entire inner tube remains in the outer tube. In both instances this could prevent the screw from being removed and used causing a surgical delay. The 25 total 2020-06-08
2014-01-27 Class II Labeling design Certain modules containing the Synthes Small Notch Titanium Reconstructive Plate set was distributed by Spine sales consultants although it was contraindicated for certain spine applications. 18747 2016-08-26
2014-01-07 Class II Component design/selection The Drill Template and the Saw Guide for the Ulna Osteotomy System may exhibit jamming, bending, or breaking of the screw connecting the Saw Guide to the Drill Template or jamming, bending, or breaking of the K-wire during fixation of the D 343 2015-09-10

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