Trigen
Trigen Trochanteric Antegrade Nail Rose 11.5MM X 50CM 130 Degree Right
17manufacturers in China registered for this device type
681catalogue numbers in this listing
11510(k) clearances naming this product code
12recalls 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.
| 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
| Listed by | Smith & Nephew, Inc., United States |
|---|---|
| FDA product code | HSB |
| Device type | Rod, Fixation, Intramedullary And Accessories |
| Device class | Class 2 |
| Regulation | 21 CFR 888.3020 |
| Establishment | Contract manufacturer, Remanufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter |
| 510(k) | K122170 |
| Record published | 2018-03-19 |
| Record revised | 2025-12-16 (version 10) |
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 |
| Supplied as a kit | Yes |
| Latex | Contains natural rubber latex |
| Label carries | lot or batch number, expiry date |
| Distribution end date | 2022-03-17 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| E0015975-1 | In distribution | |
| 71645445 | In distribution | |
| 71640734 | In distribution | |
| E0015267-1 | In distribution | |
| E0017769-1 | In distribution | |
| 71631132 | In distribution | |
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| E0017905-1 | In distribution | |
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| E0016642-1 | In distribution | |
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| E0017947-1 | In distribution | |
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Showing 250 of 300 catalogue numbers.
Same 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 |
| 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 |
| Precice® Bone Transport System | NuVasive Specialized Orthopedics, Inc. | 546 |
Showing 12 of 2,207. All products under Rod, Fixation, Intramedullary And Accessories
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K243364 | 2024-12-09 |
| K210980 | 2022-11-14 |
| K163653 | 2017-10-13 |
| K161264 | 2016-11-23 |
| K122170 | 2012-10-19 |
| K111025 | 2011-07-01 |
| K092748 | 2010-04-26 |
| K043052 | 2004-11-24 |
| K040929 | 2004-05-25 |
| K040462 | 2004-03-23 |
| K032722 | 2003-10-01 |
Recalls Naming This Product
13 recalls name this product by its own identifiers, the 510(k) it is cleared under.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|---|---|
| Smith & Nephew, Inc. | 510(k) number | 2026-03-16 | Class II | Process control | Humeral nail due to a manufacturing error is missing distal holes and if implanted may lead to revision surgery but, if the missing holes are identified before implantation, an equivalent backup can be used, or a bent nail of the same size, | 5 | |
| Smith & Nephew, Inc. | 510(k) number | 2025-03-18 | Class II | Process control | Integrated Lag/Compression Screw Kit has a compression screw with hexagon socket that may be undersized, which causes the screw to be non-functional, which would require replacement with another adequate size screw, and exchange may exceed | 75 | |
| Smith & Nephew, Inc. | 510(k) number | 2023-07-24 | Class II | Process control | A complaint was received indicating that a package contained a TRIGEN TROCHANTERIC ANTEGRADE NAIL LIME 11.5MM X 40CM 130 DEGREE LEFT implant instead of a TRIGEN TROCHANTERIC ANTEGRADE NAIL LIME 11.5MM X 36CM 130 DEGREE LEFT as described on | 30 units | |
| Smith & Nephew, Inc. | 510(k) number | 2023-07-24 | Class II | Process control | A complaint was received indicating that a package contained a TRIGEN TROCHANTERIC ANTEGRADE NAIL LIME 11.5MM X 40CM 130 DEGREE LEFT implant instead of a TRIGEN TROCHANTERIC ANTEGRADE NAIL LIME 11.5MM X 36CM 130 DEGREE LEFT as described on | 32 units | |
| Smith & Nephew, Inc. | 510(k) number | 2013-03-06 | Class II | Process control | One batch of 4.5 mm diameter Trigen Low-Profile Bone Screws were incorrectly anodized with a gold coating (indicating a 5 mm diameter) instead of a gray coating (indicating a 4.5 mm diameter). | 23 units | 2019-08-16 |
| Smith & Nephew, Inc. | 510(k) number | 2010-10-15 | Not classified | Other | Targeting software has been found to provide erroneous targeting when used with the 13 mm TAN/FAN Left nails. | 445 units | 2011-02-17 |
| Smith & Nephew, Inc. | 510(k) number | 2008-04-22 | Not classified | Process control | One of the distal locking screw holes on a hindfoot fusion nail was drilled with an incorrect trajectory. | 8 | 2010-05-28 |
| Smith & Nephew, Inc. | 510(k) number | 2008-04-22 | Not classified | Process control | One of the distal locking screw holes on a hindfoot fusion nail was drilled with an incorrect trajectory. | 34 | 2010-05-28 |
| Smith & Nephew, Inc. | 510(k) number | 2008-04-22 | Not classified | Process control | One of the distal locking screw holes on a hindfoot fusion nail was drilled with an incorrect trajectory. | 45 | 2010-05-28 |
| Smith & Nephew, Inc. | 510(k) number | 2008-04-22 | Not classified | Process control | One of the distal locking screw holes on a hindfoot fusion nail was drilled with an incorrect trajectory. | 8 | 2010-05-28 |
| Smith & Nephew, Inc. | 510(k) number | 2008-04-22 | Not classified | Process control | One of the distal locking screw holes on a hindfoot fusion nail was drilled with an incorrect trajectory. | 40 | 2010-05-28 |
| Smith & Nephew, Inc. | 510(k) number | 2008-04-22 | Not classified | Process control | One of the distal locking screw holes on a hindfoot fusion nail was drilled with an incorrect trajectory. | 114 | 2010-05-28 |
| Smith & Nephew, Inc. | 510(k) number | 2008-04-22 | Not classified | Process control | One of the distal locking screw holes on a hindfoot fusion nail was drilled with an incorrect trajectory. | 16 | 2010-05-28 |
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.