PediLoc Fragment System

PediLoc Fragment System is a range of plates, screws and instruments for temporary internal bone fixation. A plate-and-screw construct holds bone segments stable while healing proceeds…

Registry build 21.09.26

PediLoc Fragment System is a range of plates, screws and instruments for temporary internal bone fixation. A plate-and-screw construct holds bone segments stable while healing proceeds after a fracture, osteotomy or other reconstructive fixation procedure.

The range serves pediatric patients other than neonates and small-stature adults. It covers long bones, small bones, the pelvis and scapula, with implant and instrument options for different fixation sites.

Listed Item

3.5mm Locking T-Plate, 3 Hole Head, 12 Hole

Implants and Placement Tools

The system combines implanted fixation parts with tools for their placement. Its material range includes medical-grade stainless steel and cobalt-chromium-molybdenum alloy; material and geometry depend on the particular component rather than the family name alone.

22manufacturers in China registered for this device type
462catalogue numbers in this listing
15510(k) clearances naming this product code
4recalls 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 PediLoc Fragment System
Listed by Orthopediatrics, Corp, United States
FDA product code HRS
Device type Plate, Fixation, Bone
Device class Class 2
Regulation 21 CFR 888.3030
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K140431
Record published 2015-08-01
Record revised 2025-11-20 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Prescription Prescription only
Label carries lot or batch number
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for PediLoc Fragment System
Catalogue number Size Status
00-1005-3010 In distribution
00-1005-4702 In distribution
00-1005-3412 In distribution
00-1005-4767 In distribution
00-1005-2306 In distribution
00-1005-3416 In distribution
00-1005-2763 In distribution
00-1005-3208 In distribution
00-1005-4843 In distribution
00-1005-2118 In distribution
00-1005-3410 In distribution
00-1005-3216 In distribution
00-1005-4729 In distribution
00-1005-2746 In distribution
00-1005-3112 In distribution
00-1005-4707 In distribution
00-1005-3860 In distribution
00-1005-3016 In distribution
00-1005-3806 In distribution
00-1005-3845 In distribution
00-1005-3824 In distribution
00-1005-3850 In distribution
00-1005-2724 In distribution
00-1005-2769 In distribution
00-1005-3702 In distribution
00-1005-3752 In distribution
00-1005-2804 In distribution
00-1005-3309 In distribution
00-1005-3818 In distribution
00-1005-2303 In distribution
00-1005-2206 In distribution
00-1005-3002 In distribution
00-1005-2805 In distribution
00-1005-2823 In distribution
00-1005-2806 In distribution
00-1005-2314 In distribution
00-1005-2714 In distribution
00-1005-2852 In distribution
00-1005-3209 In distribution
00-1005-3304 In distribution
00-1005-3809 In distribution
00-1005-2756 In distribution
00-1005-2205 In distribution
00-1005-2830 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
K260323 2026-04-30
K252600 2025-10-09
K243963 2025-04-29
K190992 2019-08-06
K172425 2017-12-06
K171173 2017-08-24
K162307 2016-09-27
K140431 2014-07-29
K110959 2011-08-05
K111086 2011-06-17
K100240 2010-05-17
K090666 2009-04-24
K083286 2009-01-30
K081407 2008-07-22
K073344 2008-02-19

Recalls

4 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
2015-07-28 Class II Packaging process control The 00-0903-2510, 3.5mm x 10mm Non Locking Cortical Screw, Lot # 150192-J package may contain a different screw. The screw in the package is a 00-0903-2526, 3.5mm x 26mm, and is etched correctly. 5 2016-03-17
2013-09-26 Class II Labeling mix-ups The firm identified, through complaints that the 3.5MM LOCKING SCREW packaging material was marked as a 3.5mm screw and the part number was correct but that the description indicated a 7.0mm screw. Upon investigation, it has been determined 7 units shipped 2013-12-26
2012-10-18 Class II Nonconforming Material/Component Complaint received from sales representative that the drill guide tubes would not screw into replenishment instrument. Upon investigation, it has been determined that the device was not manufactured to design specifications and will not fun 24 2013-09-18
2012-06-14 Class II Error in labeling The device is a Left 8 hole plate but is incorrectly labeled and etched as a Right device. 15 devices 2013-04-30

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