Scfe Screw

3.5mm X 50mm MEDIUM THREADED CANNULATED CANCELLOUS SCREW

Registry build 21.09.26
22manufacturers in China registered for this device type
159catalogue 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 Scfe Screw
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) K082949
Record published 2015-10-13
Record revised 2024-02-19 (version 4)

Specifications

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

Catalogue Numbers

Catalogue numbers for Scfe Screw
Catalogue number Size Status
00-1071-7050 In distribution
00-1071-8238 In distribution
00-1071-7030 In distribution
00-1071-6034 In distribution
00-1071-1100 In distribution
00-1071-1065 In distribution
00-1071-3045 In distribution
00-1071-1050 In distribution
00-1071-5034 In distribution
00-1071-5014 In distribution
00-1071-1095 In distribution
00-1071-6026 In distribution
00-1071-1075 In distribution
00-1071-4028 In distribution
00-1071-4014 In distribution
00-1071-3030 In distribution
00-1071-5012 In distribution
00-1071-6016 In distribution
00-1071-4032 In distribution
00-1071-2090 In distribution
00-1071-1055 In distribution
00-1071-1110 In distribution
00-1071-6032 In distribution
00-1071-5019 In distribution
00-1071-4038 In distribution
00-1071-3060 In distribution
00-1071-8212 In distribution
00-1071-8228 In distribution
00-1071-2105 In distribution
00-1071-2065 In distribution
00-1071-1080 In distribution
00-1071-8250 In distribution
00-1071-8246 In distribution
00-1071-7032 In distribution
00-1071-8242 In distribution
00-1071-4040 In distribution
00-1071-2070 In distribution
00-1071-5021 In distribution
00-1071-4017 In distribution
00-1071-2100 In distribution
00-1071-3110 In distribution
00-1071-8218 In distribution
00-1071-8216 In distribution
00-1071-7048 In distribution
00-1071-7038 In distribution
00-1071-5050 In distribution
00-1071-1045 In distribution
00-1071-8255 In distribution
00-1071-4026 In distribution
00-1071-6018 In distribution
00-1071-2120 In distribution
00-1071-5020 In distribution
00-1071-3100 In distribution
00-1071-8214 In distribution
00-1071-5010 In distribution
00-1071-4045 In distribution
00-1071-1120 In distribution
00-1071-7055 In distribution
00-1071-1105 In distribution
00-1071-6022 In distribution
00-1071-4036 In distribution
00-1071-5028 In distribution
00-1071-3095 In distribution
00-1071-8210 In distribution
00-1071-2075 In distribution
00-1071-8230 In distribution
00-1071-8222 In distribution
00-1071-8232 In distribution
00-1071-1085 In distribution
00-1071-6020 In distribution
00-1071-1030 In distribution
00-1071-6042 In distribution
00-1071-4022 In distribution
00-1071-3065 In distribution
00-1071-3115 In distribution
00-1071-8220 In distribution
00-1071-3105 In distribution
00-1071-3050 In distribution
00-1071-1040 In distribution
00-1071-2110 In distribution
00-1071-2115 In distribution
00-1071-6060 In distribution
00-1071-8244 In distribution
00-1071-5024 In distribution
00-1071-3070 In distribution
00-1071-3075 In distribution
00-1071-3055 In distribution
00-1071-5022 In distribution
00-1071-6048 In distribution
00-1071-6028 In distribution
00-1071-7040 In distribution
00-1071-8234 In distribution
00-1071-4018 In distribution
00-1071-1070 In distribution
00-1071-5040 In distribution
00-1071-1035 In distribution
00-1071-1060 In distribution
00-1071-2080 In distribution
00-1071-6055 In distribution
00-1071-3090 In distribution
00-1071-2050 In distribution
00-1071-2055 In distribution
00-1071-4021 In distribution
00-1071-2095 In distribution
00-1071-6014 In distribution
00-1071-5018 In distribution
00-1071-6010 In distribution
00-1071-6024 In distribution
00-1071-6050 In distribution
00-1071-8226 In distribution
00-1071-5013 In distribution
00-1071-4034 In distribution
00-1071-6030 In distribution
00-1071-6036 In distribution
00-1071-7036 In distribution
00-1071-4023 In distribution
00-1071-8248 In distribution
00-1071-3120 In distribution
00-1071-4020 In distribution
00-1071-3085 In distribution
00-1071-4019 In distribution
00-1071-4016 In distribution
00-1071-6038 In distribution
00-1071-000 In distribution
00-1071-6040 In distribution
00-1071-5011 In distribution
00-1071-4015 In distribution
00-1071-5038 In distribution
00-1071-4024 In distribution
00-1071-1115 In distribution
00-1071-2060 In distribution
00-1071-5016 In distribution
00-1071-3040 In distribution
00-1071-8224 In distribution
00-1071-5045 In distribution
00-1071-7034 In distribution
00-1071-3080 In distribution
00-1071-7042 In distribution
00-1071-5026 In distribution
00-1071-6046 In distribution
00-1071-6044 In distribution
00-1071-2085 In distribution
00-1071-7060 In distribution
00-1071-5023 In distribution
00-1071-5015 In distribution
00-1071-4050 In distribution
00-1071-8236 In distribution
00-1071-4030 In distribution
00-1071-5017 In distribution
00-1071-5032 In distribution
00-1071-5030 In distribution
00-1071-8240 In distribution
00-1071-5036 In distribution
00-1071-3035 In distribution
00-1071-1090 In distribution
00-1071-6012 In distribution
00-1071-7046 In distribution
00-1071-7044 In distribution
00-1071-8260 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
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