Pin, Fixation, Smooth

Steinmann PIN Diamond Point Chuck END 5/64 X 9

Registry build 21.09.26
12manufacturers in China registered for this device type
91catalogue numbers in this listing
1510(k) clearance
3recalls on this code

Who Else Makes It

Concentrated in Jiangsu (5), Shanghai (3), Zhejiang (2). 7 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HTY
Manufacturer City Province Registered as Device types
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 Ahno Medical Devices Co., Ltd. Suzhou Jiangsu Contract manufacturer 17
Suzhou Kangli Orthopaedics Instrument Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 11
Kingj Medical Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 7
Aplus (Guangzhou) Medical Technology Company Guangzhou Guangdong Contract manufacturer 6
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Arthrex (Shanghai) Co., Ltd. Shanghai Shanghai Exporter 38

Record

Regulatory record for Pin, Fixation, Smooth
Listed by Smith & Nephew, Inc., United States
FDA product code HTY
Device type Pin, Fixation, Smooth
Device class Class 2
Regulation 21 CFR 888.3040
Establishment Contract manufacturer, Remanufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K863734
Record published 2015-08-29
Record revised 2025-12-19 (version 7)

Specifications

Specifications
MRI safety MR Conditional
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Packaging Box of 6
Distribution end date 2020-08-04
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Pin, Fixation, Smooth
Catalogue number Size Per pack Status
128119 In distribution
128078 In distribution
128022 6 In distribution
128097 In distribution
72204572 In distribution
71929134 In distribution
128077 In distribution
128040 6 In distribution
128079 In distribution
128076 In distribution
128061 6 In distribution
72204571 In distribution
128031 In distribution
128136 In distribution
128012 6 In distribution
919261 In distribution
128120 In distribution
128098 In distribution
128140 In distribution
128051 In distribution
128141 In distribution
128138 In distribution
128100 In distribution
72204566 In distribution
128020 6 In distribution
128087 In distribution
128145 In distribution
128010 In distribution
128131 In distribution
128101 In distribution
128109 In distribution
128129 In distribution
128054 6 In distribution
128126 In distribution
128021 6 In distribution
128057 6 In distribution
128081 In distribution
128110 In distribution
128088 In distribution
128106 In distribution
128041 6 In distribution
128111 In distribution
128117 In distribution
128137 In distribution
128099 In distribution
128062 6 In distribution
128192 In distribution
128118 In distribution
128096 In distribution
128005 In distribution
128127 In distribution
128017 6 In distribution
128050 In distribution
128032 6 In distribution
128090 In distribution
128146 In distribution
128060 6 In distribution
128007 6 In distribution
128108 In distribution
128107 In distribution
128052 6 In distribution
128089 In distribution
128139 In distribution
128037 6 In distribution
128116 In distribution
128086 In distribution
128520 In distribution
128030 In distribution
128011 In distribution
128044 6 In distribution
128034 6 In distribution
72204574 In distribution
128518 In distribution
128091 In distribution
128080 In distribution
128042 6 In distribution
128064 6 In distribution
128121 In distribution
128130 In distribution
128128 In distribution
72204573 Withdrawn
72204564 Withdrawn
72204565 Withdrawn
72204581 Withdrawn
72204569 Withdrawn
72204583 Withdrawn
72204575 Withdrawn
72204586 Withdrawn
72204584 Withdrawn
72204567 Withdrawn
72204578 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Rondo’ Citieffe SRL 265
HNM Medical HNM Stainless, LLC. 232
Kmedic Teleflex Medical LLC 227
gSource Gsource, LLC. 221
MicroAire® Microaire Surgical Instruments LLC 213
Orthomed Ortho-MED, Inc. 163
mahe medical GmbH Mahe Intl., Inc. 160
Pin, Fixation, Smooth Key Surgical, LLC 134
Pin, Fixation, Smooth Stryker GmbH 134
Aptus Medartis Inc. 134
Key Surgical K-Wires and Steinmann Pins Key Surgical, LLC 126
PedFlex Flexible Nailing System Orthopediatrics, Corp 119

Showing 12 of 682. All products under Pin, Fixation, Smooth

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K041355 2004-07-30

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of Pin, Fixation, Smooth
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Microaire Surgical Instruments LLC 510(k) number 2017-02-21 Class II Labeling mix-ups Mislabeling on three lots of K-Wires. The incorrect product description ” dual trocar” instead of “single trocar” was on the product label on the following parts: 1600-9355NS (lot 61005), 1600-9625NS (lot 60297), and 1604-162NS (lot 62856) Total 362 2017-07-14

Recalls

2 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
2024-07-09 Class II Packaging change control Smith & Nephew, Inc., has initiated a field action to voluntarily remove two batches of K-Wires due to a packaging error. A complaint was received indicating that a package contained K-WIRE.062X9 2PT DM wires instead of K-WIRE.045X9 2PT D 73 units
2024-07-09 Class II Packaging change control Smith & Nephew, Inc., has initiated a field action to voluntarily remove two batches of K-Wires due to a packaging error. A complaint was received indicating that a package contained K-WIRE.062X9 2PT DM wires instead of K-WIRE.045X9 2PT D 24 units
2010-06-28 Not classified Process control Plastic trays which encase these products have burrs on the hinged packaging which can puncture the single barrier sterile pouch, compromising sterility. 8 units 2012-01-23

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