Arsenal Foot

3.5mm x 32mm Arsenal Locking Screw

Registry build 21.09.26
31manufacturers in China registered for this device type
172catalogue numbers in this listing
7510(k) clearances naming this product code
15recalls 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 Arsenal Foot
Listed by Trilliant Surgical LLC, United States
FDA product code HWC
Device type Screw, Fixation, Bone
Device class Class 2
Regulation 21 CFR 888.3040
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K191009
Record published 2019-10-01
Record revised 2025-08-13 (version 5)

Specifications

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

Catalogue Numbers

Catalogue numbers for Arsenal Foot
Catalogue number Size Status
307-22-026 In distribution
308-35-032 In distribution
308-40-034 In distribution
307-35-050 In distribution
307-40-020 In distribution
308-27-044 In distribution
308-35-070 In distribution
307-22-018 In distribution
307-40-026 In distribution
307-27-020 In distribution
307-27-038 In distribution
307-40-065 In distribution
307-35-048 In distribution
308-40-042 In distribution
308-27-024 In distribution
308-27-036 In distribution
307-40-028 In distribution
307-35-038 In distribution
308-22-010 In distribution
308-27-008 In distribution
308-35-042 In distribution
308-40-022 In distribution
308-22-028 In distribution
308-35-024 In distribution
308-35-010 In distribution
307-22-024 In distribution
308-35-018 In distribution
307-35-055 In distribution
307-40-038 In distribution
307-35-036 In distribution
307-40-044 In distribution
308-35-022 In distribution
308-22-012 In distribution
308-40-070 In distribution
307-27-030 In distribution
308-40-044 In distribution
308-35-030 In distribution
308-22-014 In distribution
308-35-008 In distribution
308-35-036 In distribution
308-22-030 In distribution
307-35-024 In distribution
307-40-050 In distribution
308-22-018 In distribution
307-40-034 In distribution
308-40-018 In distribution
307-40-060 In distribution
307-40-040 In distribution
308-27-034 In distribution
308-40-038 In distribution
307-27-032 In distribution
307-40-048 In distribution
307-35-046 In distribution
307-35-040 In distribution
307-22-016 In distribution
308-27-050 In distribution
307-22-020 In distribution
308-35-048 In distribution
307-35-020 In distribution
308-22-026 In distribution
307-27-048 In distribution
307-35-044 In distribution
307-27-014 In distribution
307-40-022 In distribution
307-35-014 In distribution
308-27-028 In distribution
308-27-016 In distribution
308-40-024 In distribution
307-40-016 In distribution
308-35-046 In distribution
307-35-028 In distribution
307-40-012 In distribution
308-40-060 In distribution
307-22-006 In distribution
308-35-060 In distribution
308-27-038 In distribution
307-22-008 In distribution
307-40-046 In distribution
308-22-022 In distribution
308-27-032 In distribution
308-35-014 In distribution
307-27-040 In distribution
308-40-028 In distribution
308-35-012 In distribution
308-35-020 In distribution
308-40-048 In distribution
307-40-030 In distribution
307-27-046 In distribution
308-35-044 In distribution
307-27-012 In distribution
308-40-040 In distribution
308-27-026 In distribution
308-22-006 In distribution
308-35-016 In distribution
307-27-018 In distribution
308-27-010 In distribution
307-27-034 In distribution
308-22-024 In distribution
307-22-010 In distribution
307-35-018 In distribution
307-40-010 In distribution
308-35-034 In distribution
307-40-014 In distribution
307-27-026 In distribution
308-40-012 In distribution
307-35-065 In distribution
307-35-010 In distribution
308-40-014 In distribution
308-27-040 In distribution
307-27-016 In distribution
308-22-020 In distribution
307-40-055 In distribution
308-40-046 In distribution
308-27-046 In distribution
307-27-010 In distribution
308-35-050 In distribution
307-27-008 In distribution
307-40-018 In distribution
308-40-026 In distribution
307-35-034 In distribution
307-35-032 In distribution
308-40-010 In distribution
307-22-012 In distribution
307-40-032 In distribution
308-40-032 In distribution
308-40-055 In distribution
308-40-030 In distribution
307-40-036 In distribution
307-22-030 In distribution
307-27-024 In distribution
308-27-018 In distribution
308-27-022 In distribution
308-40-065 In distribution
308-27-042 In distribution
308-35-055 In distribution
307-35-042 In distribution
307-22-022 In distribution
307-35-008 In distribution
307-40-070 In distribution
308-27-012 In distribution
307-35-016 In distribution
308-40-050 In distribution
307-27-050 In distribution
307-35-070 In distribution
308-27-030 In distribution
307-27-028 In distribution
307-27-044 In distribution
307-35-012 In distribution
308-22-008 In distribution
308-40-036 In distribution
307-22-028 In distribution
307-35-060 In distribution
308-40-020 In distribution
307-40-024 In distribution
308-40-016 In distribution
308-35-028 In distribution
308-35-026 In distribution
307-27-022 In distribution
308-27-048 In distribution
308-35-038 In distribution
307-35-026 In distribution
307-40-042 In distribution
307-35-030 In distribution
308-35-065 In distribution
307-35-022 In distribution
308-35-040 In distribution
308-27-014 In distribution
307-22-014 In distribution
307-27-036 In distribution
308-27-020 In distribution
308-22-016 In distribution
307-27-042 In distribution

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
K181898 2018-10-26
K153338 2016-01-14
K122959 2012-11-07
K111834 2011-12-06
K112737 2011-10-20
K103183 2011-02-08
K081510 2008-08-04

Recalls

14 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
2018-07-19 Class II Labeling Change Control Instructions for Use (IFU) and Surgical Cleaning and Sterilization Protocols updated with revised dry time parameters. This recall of IFU occurred in 2018. 3 systems
2018-07-19 Class II Labeling Change Control Instructions for Use (IFU) and Surgical Cleaning and Sterilization Protocols updated with revised dry time parameters. This recall of IFU occurred in 2018. 170 systems
2018-07-19 Class II Labeling Change Control Instructions for Use (IFU) and Surgical Cleaning and Sterilization Protocols updated with revised dry time parameters. This recall of IFU occurred in 2018. 4 systems total for both Disco Sublatar and Twist Sublatar
2018-07-19 Class II Labeling Change Control Instructions for Use (IFU) and Surgical Cleaning and Sterilization Protocols updated with revised dry time parameters. This recall of IFU occurred in 2018. 2 systems
2018-07-19 Class II Labeling Change Control Instructions for Use (IFU) and Surgical Cleaning and Sterilization Protocols updated with revised dry time parameters. This recall of IFU occurred in 2018. 9 systems
2018-07-19 Class II Labeling Change Control Instructions for Use (IFU) and Surgical Cleaning and Sterilization Protocols updated with revised dry time parameters. This recall of IFU occurred in 2018. 4 systems total for both Twist Sublatar and Disco Sublatar
2018-07-19 Class II Labeling Change Control Instructions for Use (IFU) and Surgical Cleaning and Sterilization Protocols updated with revised dry time parameters. This recall of IFU occurred in 2018. 4 systems
2018-07-19 Class II Labeling Change Control Instructions for Use (IFU) and Surgical Cleaning and Sterilization Protocols updated with revised dry time parameters. This recall of IFU occurred in 2018. 17 systems
2018-07-19 Class II Labeling Change Control Instructions for Use (IFU) and Surgical Cleaning and Sterilization Protocols updated with revised dry time parameters. This recall of IFU occurred in 2018. 28 systems
2018-07-19 Class II Labeling Change Control Instructions for Use (IFU) and Surgical Cleaning and Sterilization Protocols updated with revised dry time parameters. This recall of IFU occurred in 2018. 8 systems
2016-12-08 Class II Under Investigation by firm Four lots of Tiger Screw Sterilization Tray Base Assemblies were released to the field with a printing error where k-wire description markings indicate diameters of 0.45 and 0.35 instead of 0.045″ and 0.035″, respectively. 50 units 2017-05-17
2016-09-02 Class II Nonconforming Material/Component Screws were identified as having the incorrect part number and lot number marked upon them. The part number incorrectly indicated a length of 115 mm rather than 110 mm. The lot number incorrectly indicated lot number of TSL003765 rather th 11 2017-05-19
2015-07-20 Class II Nonconforming Material/Component The cutting efficiency of the Countersinks was out of specification. 102 units 2017-01-26
2015-07-20 Class II Component design/selection Sterilization tray lids for the Tiger and Tiger Headless Cannulated Screw Systems were reported to occasionally be difficult to remove from the sterilization tray. 71 units 2017-01-26
2009-04-14 Not classified Other Firm received several complaints of field failures, e.g., “broke during surgery” and the firm initiated a design change. A communication to sales staff 04/14/2009 instructed them to recover and reconcile these products from user physicians. 32 units 2010-05-03

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