TFN-Advance

11MM/135 DEG TI Cann Tfna 340MM/RIGHT - Sterile

Registry build 21.09.26
17manufacturers in China registered for this device type
343catalogue numbers in this listing
4recalls on this code

Who Else Makes It

Concentrated in Jiangsu (7), Shanghai (3), Zhejiang (3). 10 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HSB
Manufacturer City Province Registered as Device types
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
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
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
Turnxon Precision Co., Ltd. Dongguan Guangdong Contract manufacturer 17
Suzhou Kangli Orthopaedics Instrument Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 11
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70

Showing 12 of 17. All 17 manufacturers in China registered for Rod, Fixation, Intramedullary And Accessories

Record

Regulatory record for TFN-Advance
Listed by Synthes Gmbh, Switzerland
FDA product code HSB
Device type Rod, Fixation, Intramedullary And Accessories
Device class Class 2
Regulation 21 CFR 888.3020
Establishment Specification developer, Manufacturer, Exporter
510(k) K131548
Record published 2015-09-14
Record revised 2026-05-21 (version 8)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for TFN-Advance
Catalogue number Size Status
04.037.263S In distribution
04.037.938S In distribution
04.038.080S In distribution
04.037.065S In distribution
04.037.264S In distribution
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04.038.115 In distribution
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04.038.425 In distribution
04.037.254S In distribution

Showing 250 of 300 catalogue numbers.

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
T2 Stryker GmbH 1,373
Autobahn Globus Medical, Inc. 1,258
Gamma Stryker GmbH 1,120
Summa Orthopaedics Femur Nail System Jeil Medical Corporation 742
Arix Femur Nail System Jeil Medical Corporation 742
Orthofix Orthofix SRL 721
Rod, Fixation, Intramedullary And Accessories Synthes Gmbh 715
Trigen Smith & Nephew, Inc. 681
Arthrex® Arthrex, Inc. 665
Precice® Intramedullary Limb Lengthening System NuVasive Specialized Orthopedics, Inc. 596
Apex Orthoxel Designated Activity Company 569
Natural Nail® Zimmer, Inc. 552

Showing 12 of 2,207. All products under Rod, Fixation, Intramedullary And Accessories

Recalls Naming This Product

9 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of TFN-Advance
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Synthes (USA) Products LLC 510(k) number 2024-01-24 Class II Process control Products not sterilized, sterility cannot be confirmed 11 units
Synthes (USA) Products LLC 510(k) number 2024-01-24 Class II Process control Products not sterilized, sterility cannot be confirmed 11 units
Synthes (USA) Products LLC 510(k) number 2023-02-01 Class II Under Investigation by firm TFNA Femoral Nails labeled and etched as 200mm may measure 170mm in length, and TFNA Femoral Nails labeled and etched as 170mm may measure 200mm in length 6 units
Synthes (USA) Products LLC 510(k) number 2023-02-01 Class II Under Investigation by firm TFNA Femoral Nails labeled and etched as 200mm may measure 170mm in length, and TFNA Femoral Nails labeled and etched as 170mm may measure 200mm in length 5 units
Synthes (USA) Products LLC 510(k) number 2023-02-01 Class II Under Investigation by firm TFNA Femoral Nails labeled and etched as 200mm may measure 170mm in length, and TFNA Femoral Nails labeled and etched as 170mm may measure 200mm in length 6 units
Synthes (USA) Products LLC 510(k) number 2015-09-21 Class II Device Design Certain lots of the Screw Inserter may be etched with incorrect graphics. The orientation of the etched image of the oblique angle on the Screw Inserter may not correspond to the tip of the angle of the instrument. 793 2016-08-26
Synthes (USA) Products LLC 510(k) number 2015-06-10 Class II Process control The height of one of the three guiding pins of the Helical Blade Inserter for the TFNA is oversized. The Helical Blade Inserter is therefore unable to pass through the Blade/Screw Guide Sleeve (part 03.037.017). 32 2016-08-18
Synthes Gmbh 510(k) number 2015-04-09 Class II Process control TFNA nails from certain lots were assembled with a locking mechanism too close to the top of the nail.

Potential patient impact: surgical delay.

8175 2016-08-18
Synthes Gmbh 510(k) number 2015-02-24 Class II Component design/selection The guide sleeve has the potential to jam in the Aiming Arms, which may delay disassembly and removal of instruments. 131 2015-09-21

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
2015-05-27 Class II Process control certain lots of the Titanium Recon Screws (6.5mm ) were found to contain the incorrect insert GP0760-A (Synthes Titanium Buttress Locking Plate System), instead of the correct insert GP0706-E (Synthes Titanium Intramedullary Nails and Compo 276 2015-12-18
2014-10-29 Class II Employee error The 10 mm/135 degree Titanium Cannulated Trochanteric Fixation Nail 170 MM (Sterile) was assembled incorrectly. If the non conformance goes undetected, it may impact the locking function post-operatively and compromise the bone reduction an 6 2015-12-18

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