3p Hip System

11.5mm Partially Threaded Adolescent Beam Screw, 110mm, Short Thread

Registry build 21.09.26
31manufacturers in China registered for this device type
452catalogue numbers in this listing
2510(k) clearances naming this product code
7recalls on this code

Who Else Makes It

Concentrated in Jiangsu (15), Shanghai (5), Zhejiang (3). 19 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HWC
Manufacturer City Province Registered as Device types
MicroPort Orthopedics Global Supply Center Limited Shanghai Shanghai Contract manufacturer 82
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
Canwell Medical Co., Ltd. Jinhua Zhejiang Contract manufacturer 42
Suzhou Elite Precision Machinery Co., Ltd. Kunshan Jiangsu Contract manufacturer 35
B-ONE Medical (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 23
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Suzhou Ahno Medical Devices Co., Ltd. Suzhou Jiangsu Contract manufacturer 17
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Sanbor Medical Xiamen, Inc. Xiamen Fujian Contract manufacturer 16
Suzhou Kangli Orthopaedics Instrument Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 11

Showing 12 of 31. All 31 manufacturers in China registered for Screw, Fixation, Bone

Record

Regulatory record for 3P Hip System
Listed by Orthopediatrics, Corp, United States
FDA product code HWC
Device type Screw, Fixation, Bone
Device class Class 2
Regulation 21 CFR 888.3040
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K243963
Record published 2025-06-19

Specifications

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

Catalogue Numbers

Catalogue numbers for 3P Hip System
Catalogue number Size Status
00-3050-0072 In distribution
00-3035-1064 In distribution
00-3035-1028 In distribution
00-3035-3055 In distribution
00-3035-0130 In distribution
00-3035-0078 In distribution
00-3050-3058 In distribution
00-3006-3110 In distribution
00-3050-1108 In distribution
00-3050-0084 In distribution
00-3035-0036 In distribution
00-3035-0032 In distribution
00-3035-0086 In distribution
00-3006-2075 In distribution
00-3050-3100 In distribution
00-3035-3062 In distribution
00-3005-3090 In distribution
00-3035-1090 In distribution
00-3050-0066 In distribution
00-3035-0025 In distribution
00-3035-0126 In distribution
00-3050-1104 In distribution
00-3006-6115 In distribution
00-3050-0115 In distribution
00-3035-0034 In distribution
00-3004-2065 In distribution
00-3050-3040 In distribution
00-3050-3120 In distribution
00-3050-0026 In distribution
00-3035-0044 In distribution
00-3050-0032 In distribution
00-3035-1008 In distribution
00-3035-1055 In distribution
00-3050-0106 In distribution
00-3004-3105 In distribution
00-3050-0122 In distribution
00-3050-3108 In distribution
00-3050-3105 In distribution
00-3035-3084 In distribution
00-3006-6065 In distribution
00-3050-1105 In distribution
00-3050-0100 In distribution
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00-3050-1038 In distribution
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00-3035-0045 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
Screw, Fixation, Bone Synthes Gmbh 3,975
Aptus Medartis Inc. 3,623
Acumed Acumed LLC 3,187
Arthrex® Arthrex, Inc. 2,781
OsteoMed Osteomed 2,764
Screw, Fixation, Bone AAP Implantate AG 2,176
Screw, Fixation, Bone Zimmer, Inc. 1,993
Arix System Bone Screw Jeil Medical Corporation 1,875
Cannulated Screw System + Tyber Medical 1,814
Cannulated Compression Headless Screw Tyber Medical 1,621
Microware Bone Plates and Bone Screws Microware Precision Co., Ltd. 1,601
Anthem Globus Medical, Inc. 1,538

Showing 12 of 5,775. All products under Screw, Fixation, Bone

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K190324 2019-07-05
K082949 2008-11-25

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
2016-07-27 Class II Labeling mix-ups OrthoPediatrics Corp.is voluntarily recalling multiple lots of the 3.5mm Bowed Locking Compression Femur 14-hole Plate and 18-hole Plate due to the devices being mislabeled. 41 2017-03-24
2016-07-27 Class II Labeling mix-ups OrthoPediatrics Corp.is voluntarily recalling multiple lots of the 3.5mm Bowed Locking Compression Femur 14-hole Plate and 18-hole Plate due to the devices being mislabeled. 41 2017-03-24
2014-01-08 Class II Labeling mix-ups OrthoPediatrics has initiated a Voluntary RECALL of Part # 00-0903-2620, 3.5MM Locking Cortical
Screw, Lot # 009SV because the device within the package may be incorrect. These packages incorrectly contain a 3.5mm Non Locking Cortical Scre
12 units 2014-04-23
2013-07-24 Class II Process design OrthoPediatrics has initiated a voluntary recall of Part # 01-1050-002, 2.5mm Drill Bit, Lot #91300335. Only drill bits that are in their original packaging are being recalled. The description on the package of this drill bit has a wrong si 68 2013-08-26
2013-04-19 Class II Device Design Post Market Surveillance of the 90 degree Cannulated Infant Blade Plate indicated that there have been five reports concerning bending of the plate intra-operatively. 130 devices were shipped 2013-09-19
2013-04-19 Class II Device Design Post Market Surveillance of the 90 degree Cannulated Infant Blade Plate indicated that there have been five reports concerning bending of the plate intra-operatively. 130 devices were shipped 2013-09-19
2013-04-19 Class II Device Design Post Market Surveillance of the 90 degree Cannulated Infant Blade Plate indicated that there have been five reports concerning bending of the plate intra-operatively. 130 devices were shipped 2013-09-19

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