Ace®trochanteric Nail
21 catalogue numbers from 9032-09-135, listed by Biomet Orthopedics, United States, under Rod, Fixation, Intramedullary And Accessories. 17 manufacturers in China are registered for this product code.
17manufacturers in China registered for this device type
21catalogue numbers in this listing
4510(k) clearances naming this product 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 | Biomet Orthopedics, United States |
|---|---|
| FDA product code | HSB |
| Device type | Rod, Fixation, Intramedullary And Accessories |
| Device class | Class 2 |
| Regulation | 21 CFR 888.3020 |
| 510(k) | K010780 |
| Record published | 2015-10-24 |
| Record revised | 2025-05-30 (version 6) |
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 number | Size | Status |
|---|---|---|
| 9032-09-135 | 135° 180MM X 9MM | In distribution |
| 9030-13-225 | 125 DEG 200MM X 13MM | In distribution |
| 9032-09-125 | 125° 180MM X 9MM | In distribution |
| 9032-13-225 | 125° 200MM X 13MM | In distribution |
| 9030-11-235 | 135 DEG 200MM X 11MM | In distribution |
| 9032-11-235 | 135° 200MM X 11MM | In distribution |
| 9032-13-230 | 130° 200MM X 13MM | In distribution |
| 9032-13-235 | 135° 200MM X 13MM | In distribution |
| 9030-13-235 | 135 DEG 200MM X 13MM | In distribution |
| 9030-11-230 | 130 DEG 200MM X 11MM | In distribution |
| 9030-11-225 | 125 DEG 200MM X 11MM | In distribution |
| 9032-11-125 | 125° 180MM X 11MM | In distribution |
| 9032-13-125 | 125° 180MM X 13MM | In distribution |
| 9032-11-130 | 130° 180MM X 11MM | In distribution |
| 9032-11-135 | 135° 180MM X 11MM | In distribution |
| 9032-11-225 | 125° 200MM X 11MM | In distribution |
| 9032-09-130 | 130° 180MM X 9MM | In distribution |
| 9032-11-230 | 130° 200MM X 11MM | In distribution |
| 9030-13-230 | 130 DEG 200MM X 13MM | In distribution |
| 9032-13-130 | 130° 180MM X 13MM | In distribution |
| 9032-13-135 | 135° 180MM X 13MM | In distribution |
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 |
| 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
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K070955 | 2007-10-12 |
| K013923 | 2002-02-25 |
| K002278 | 2000-10-23 |
| K002057 | 2000-10-04 |
Recalls Naming This Product
85 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 |
|---|---|---|---|---|---|---|---|
| Biomet, Inc. | 510(k) number | 2017-12-20 | Class II | Device Design | Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric Nail (ATN) system after a Device Performance Review (DPR) failed clinical analysis for survivorship pursuant to the acceptance criteria for the DPR protocol for th | 3454 | 2020-04-22 |
| Biomet, Inc. | 510(k) number | 2017-12-20 | Class II | Device Design | Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric Nail (ATN) system after a Device Performance Review (DPR) failed clinical analysis for survivorship pursuant to the acceptance criteria for the DPR protocol for th | 3454 | 2020-04-22 |
| Biomet, Inc. | 510(k) number | 2017-12-20 | Class II | Device Design | Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric Nail (ATN) system after a Device Performance Review (DPR) failed clinical analysis for survivorship pursuant to the acceptance criteria for the DPR protocol for th | 3454 | 2020-04-22 |
| Biomet, Inc. | 510(k) number | 2017-12-20 | Class II | Device Design | Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric Nail (ATN) system after a Device Performance Review (DPR) failed clinical analysis for survivorship pursuant to the acceptance criteria for the DPR protocol for th | 3454 | 2020-04-22 |
| Biomet, Inc. | 510(k) number | 2017-12-20 | Class II | Device Design | Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric Nail (ATN) system after a Device Performance Review (DPR) failed clinical analysis for survivorship pursuant to the acceptance criteria for the DPR protocol for th | 3454 | 2020-04-22 |
| Biomet, Inc. | 510(k) number | 2017-12-20 | Class II | Device Design | Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric Nail (ATN) system after a Device Performance Review (DPR) failed clinical analysis for survivorship pursuant to the acceptance criteria for the DPR protocol for th | 3454 | 2020-04-22 |
| Biomet, Inc. | 510(k) number | 2017-12-20 | Class II | Device Design | Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric Nail (ATN) system after a Device Performance Review (DPR) failed clinical analysis for survivorship pursuant to the acceptance criteria for the DPR protocol for th | 3454 | 2020-04-22 |
| Biomet, Inc. | 510(k) number | 2017-12-20 | Class II | Device Design | Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric Nail (ATN) system after a Device Performance Review (DPR) failed clinical analysis for survivorship pursuant to the acceptance criteria for the DPR protocol for th | 3454 | 2020-04-22 |
| Biomet, Inc. | 510(k) number | 2017-12-20 | Class II | Device Design | Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric Nail (ATN) system after a Device Performance Review (DPR) failed clinical analysis for survivorship pursuant to the acceptance criteria for the DPR protocol for th | 3454 | 2020-04-22 |
| Biomet, Inc. | 510(k) number | 2017-12-20 | Class II | Device Design | Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric Nail (ATN) system after a Device Performance Review (DPR) failed clinical analysis for survivorship pursuant to the acceptance criteria for the DPR protocol for th | 3454 | 2020-04-22 |
| Biomet, Inc. | 510(k) number | 2017-12-20 | Class II | Device Design | Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric Nail (ATN) system after a Device Performance Review (DPR) failed clinical analysis for survivorship pursuant to the acceptance criteria for the DPR protocol for th | 3454 | 2020-04-22 |
| Biomet, Inc. | 510(k) number | 2016-04-01 | Class II | Equipment maintenance | Insufficient seal strength on sterile barrier packaging. The seal could be jeopardized causing the sterile barrier to be compromised and the product could become nonsterile. If the product becomes non-sterile and is used or implanted, it ma | 2017-05-23 | |
| Depuy Orthopaedics, Inc. | 510(k) number | 2003-12-11 | Not classified | Other | The lag screw may migrate to the femoral head or into the abdominal cavity. | 2004-04-15 | |
| Depuy Orthopaedics, Inc. | 510(k) number | 2003-12-11 | Not classified | Other | The lag screw may migrate to the femoral head or into the abdominal cavity. | 2004-04-15 | |
| Depuy Orthopaedics, Inc. | 510(k) number | 2003-12-11 | Not classified | Other | The lag screw may migrate to the femoral head or into the abdominal cavity. | 2004-04-15 | |
| Depuy Orthopaedics, Inc. | 510(k) number | 2003-12-11 | Not classified | Other | The lag screw may migrate to the femoral head or into the abdominal cavity. | 2004-04-15 | |
| Depuy Orthopaedics, Inc. | 510(k) number | 2003-12-11 | Not classified | Other | The lag screw may migrate to the femoral head or into the abdominal cavity. | 2004-04-15 | |
| Depuy Orthopaedics, Inc. | 510(k) number | 2003-12-11 | Not classified | Other | The lag screw may migrate to the femoral head or into the abdominal cavity. | 2004-04-15 | |
| Depuy Orthopaedics, Inc. | 510(k) number | 2003-12-11 | Not classified | Other | The lag screw may migrate to the femoral head or into the abdominal cavity. | 2004-04-15 | |
| Depuy Orthopaedics, Inc. | 510(k) number | 2003-12-11 | Not classified | Other | The lag screw may migrate to the femoral head or into the abdominal cavity. | 2004-04-15 | |
| Depuy Orthopaedics, Inc. | 510(k) number | 2003-12-11 | Not classified | Other | The lag screw may migrate to the femoral head or into the abdominal cavity. | 2004-04-15 | |
| Depuy Orthopaedics, Inc. | 510(k) number | 2003-12-11 | Not classified | Other | The lag screw may migrate to the femoral head or into the abdominal cavity. | 2004-04-15 | |
| Depuy Orthopaedics, Inc. | 510(k) number | 2003-12-11 | Not classified | Other | The lag screw may migrate to the femoral head or into the abdominal cavity. | 2004-04-15 | |
| Depuy Orthopaedics, Inc. | 510(k) number | 2003-12-11 | Not classified | Other | The lag screw may migrate to the femoral head or into the abdominal cavity. | 2004-04-15 | |
| Depuy Orthopaedics, Inc. | 510(k) number | 2003-12-11 | Not classified | Other | The lag screw may migrate to the femoral head or into the abdominal cavity. | 2004-04-15 | |
| Depuy Orthopaedics, Inc. | 510(k) number | 2003-12-11 | Not classified | Other | The lag screw may migrate to the femoral head or into the abdominal cavity. | 2004-04-15 | |
| Depuy Orthopaedics, Inc. | 510(k) number | 2003-12-11 | Not classified | Other | The lag screw may migrate to the femoral head or into the abdominal cavity. | 2004-04-15 | |
| Depuy Orthopaedics, Inc. | 510(k) number | 2003-12-11 | Not classified | Other | The lag screw may migrate to the femoral head or into the abdominal cavity. | 2004-04-15 | |
| Depuy Orthopaedics, Inc. | 510(k) number | 2003-12-11 | Not classified | Other | The lag screw may migrate to the femoral head or into the abdominal cavity. | 2004-04-15 | |
| Depuy Orthopaedics, Inc. | 510(k) number | 2003-12-11 | Not classified | Other | The lag screw may migrate to the femoral head or into the abdominal cavity. | 2004-04-15 | |
| Depuy Orthopaedics, Inc. | 510(k) number | 2003-12-11 | Not classified | Other | The lag screw may migrate to the femoral head or into the abdominal cavity. | 2004-04-15 | |
| Depuy Orthopaedics, Inc. | 510(k) number | 2003-12-11 | Not classified | Other | The lag screw may migrate to the femoral head or into the abdominal cavity. | 2004-04-15 | |
| Depuy Orthopaedics, Inc. | 510(k) number | 2003-12-11 | Not classified | Other | The lag screw may migrate to the femoral head or into the abdominal cavity. | 2004-04-15 | |
| Depuy Orthopaedics, Inc. | 510(k) number | 2003-12-11 | Not classified | Other | The lag screw may migrate to the femoral head or into the abdominal cavity. | 2004-04-15 | |
| Depuy Orthopaedics, Inc. | 510(k) number | 2003-12-11 | Not classified | Other | The lag screw may migrate to the femoral head or into the abdominal cavity. | 2004-04-15 | |
| Depuy Orthopaedics, Inc. | 510(k) number | 2003-12-11 | Not classified | Other | The lag screw may migrate to the femoral head or into the abdominal cavity. | 2004-04-15 | |
| Depuy Orthopaedics, Inc. | 510(k) number | 2003-12-11 | Not classified | Other | The lag screw may migrate to the femoral head or into the abdominal cavity. | 2004-04-15 | |
| Depuy Orthopaedics, Inc. | 510(k) number | 2003-12-11 | Not classified | Other | The lag screw may migrate to the femoral head or into the abdominal cavity. | 2004-04-15 | |
| Depuy Orthopaedics, Inc. | 510(k) number | 2003-12-11 | Not classified | Other | The lag screw may migrate to the femoral head or into the abdominal cavity. | 2004-04-15 | |
| Depuy Orthopaedics, Inc. | 510(k) number | 2003-12-11 | Not classified | Other | The lag screw may migrate to the femoral head or into the abdominal cavity. | 2004-04-15 |
Showing 40 of 85.
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.