Implant Partners
Poly 15DG Liner 36MM GRP E A-Class® Implant Partners™
15manufacturers in China registered for this device type
35catalogue numbers in this listing
12510(k) clearances naming this product code
8recalls on this code
Who Else Makes It
Concentrated in Jiangsu (8), Shanghai (3), Zhejiang (2). 10 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| MicroPort Orthopedics Global Supply Center Limited | Shanghai | Shanghai | Contract manufacturer | 82 |
| Zhejiang Biomet Medical Products Co., Ltd. | Jinhua | Zhejiang | Contract manufacturer | 74 |
| 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 |
| Stryker (Suzhou) Medical Technology Co., Ltd. | Suzhou | Jiangsu | Contract manufacturer | 19 |
| APS Materials Suzhou | Suzhou | Jiangsu | Contract manufacturer | 18 |
| Xian Airfoil Technology Co., Ltd. | Xian | Shaanxi | Contract manufacturer | 8 |
| Lincotek (Wuxi) Co., Ltd. | Wuxi | Jiangsu | Contract manufacturer | 7 |
| b-ONE Medical (Beijing) Co., Ltd. | Beijing | Beijing | Contract manufacturer | 7 |
| 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 15. All 15 manufacturers in China registered for Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
Record
| Listed by | Microport Orthopedics Inc., United States |
|---|---|
| FDA product code | LZO |
| Device type | Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented |
| Device class | Class 2 |
| Regulation | 21 CFR 888.3353 |
| Establishment | Contract manufacturer, Reprocessor, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter |
| Record published | 2015-10-23 |
| Record revised | 2018-03-29 (version 2) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, expiry date, manufacturing date |
| Sizes | Lumen/inner diameter 28 to 36 mm; outer diameter 46 to 66 mm |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| PRTLE023WD | In distribution | |
| PRTLS027WD | In distribution | |
| DLXPLE36WD | Lumen/Inner Diameter 36 mm | In distribution |
| DSPCGG60WD | Outer Diameter 60 mm | In distribution |
| PRTLS025WD | In distribution | |
| DLXPGE36WD | Lumen/Inner Diameter 36 mm | In distribution |
| DLXPLD36WD | Lumen/Inner Diameter 36 mm | In distribution |
| DLXPGF36WD | Lumen/Inner Diameter 36 mm | In distribution |
| PRTLS029WD | In distribution | |
| DLXPLG36WD | Lumen/Inner Diameter 36 mm | In distribution |
| DSPCGC50WD | Outer Diameter 50 mm | In distribution |
| PRTLS030WD | In distribution | |
| DLXPLF36WD | Lumen/Inner Diameter 36 mm | In distribution |
| PRTLE031WD | In distribution | |
| PRTLE025WD | In distribution | |
| DSPCGH64WD | Outer Diameter 64 mm | In distribution |
| DSPCGE54WD | Outer Diameter 54 mm | In distribution |
| PRTLS021WD | In distribution | |
| DSPCGB48WD | Outer Diameter 48 mm | In distribution |
| DSPCGF56WD | Outer Diameter 56 mm | In distribution |
| DSPCGG58WD | Outer Diameter 58 mm | In distribution |
| DLXPLH36WD | Lumen/Inner Diameter 36 mm | In distribution |
| DSPCGG62WD | Outer Diameter 62 mm | In distribution |
| DLXPGC32WD | Lumen/Inner Diameter 32 mm | In distribution |
| PRTLE027WD | In distribution | |
| DSPCGD52WD | Outer Diameter 52 mm | In distribution |
| DLXPLC32WD | Lumen/Inner Diameter 32 mm | In distribution |
| DLXPGD36WD | Lumen/Inner Diameter 36 mm | In distribution |
| DSPCGB46WD | Outer Diameter 46 mm | In distribution |
| DLXPGB28WD | Lumen/Inner Diameter 28 mm | In distribution |
| DSPCGH66WD | Outer Diameter 66 mm | In distribution |
| PRTLS023WD | In distribution | |
| PRTLE021WD | In distribution | |
| DLXPLB28WD | Lumen/Inner Diameter 28 mm | In distribution |
| PRTLE029WD | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Libertas | Maxx Orthopedics Inc. | 1,832 |
| Redapt | Smith & Nephew, Inc. | 326 |
| Bencox Hip System | Corentec Co., Ltd. | 295 |
| M-Vizion Femoral Revision System | Medacta International SA | 289 |
| Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented | Zimmer, Inc. | 280 |
| Profemur® | Microport Orthopedics Inc. | 229 |
| DJO Surgical | Encore Medical, L.P. | 162 |
| Instrument | Howmedica Osteonics Corp | 152 |
| Alteon | Exactech, Inc. | 151 |
| Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented | Exactech, Inc. | 136 |
| Resolve Modular Revision Hip Stem | United Orthopedic Corp. | 136 |
| Wagner SL Revision® | Zimmer, Inc. | 133 |
Showing 12 of 691. All products under Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K250444 | 2025-05-15 |
| K240452 | 2024-04-12 |
| K200007 | 2020-04-25 |
| K191632 | 2019-10-07 |
| K181598 | 2018-09-14 |
| K173776 | 2018-07-06 |
| K171181 | 2017-08-28 |
| K150133 | 2015-04-20 |
| K150302 | 2015-04-10 |
| K141235 | 2014-09-12 |
| K140676 | 2014-05-30 |
| K140043 | 2014-04-03 |
Recalls
1 of these is Class II. Class II means a temporary or reversible health consequence. Class III is unlikely to cause harm at all → typically a labelling or documentation fault. Volume alone is not a quality signal: a manufacturer that ships more recalls more.
| Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|
| 2016-11-17 | Class II | Process control | The recall is being initiated because all broach handles in the affected lot had the same non-conformity with the connection feature. The broach handles may have machining issues that do not allow the handle to properly mate with an associa | 20 units | 2018-08-18 |
| 2016-06-21 | Class III | Device Design | Revision rate trends from within the MicroPort Orthopedics Inc. database evaluated for the modular head Metal on Metal THA systems show an increasing overall trend from 2009 to present and it was found that there was a specific hazard/harm | 108,362 units | 2017-07-01 |
| 2016-06-21 | Class III | Device Design | Revision rate trends from within the MicroPort Orthopedics Inc. database evaluated for the modular head Metal on Metal THA systems show an increasing overall trend from 2009 to present and it was found that there was a specific hazard/harm | 68,221 units | 2017-07-01 |
| 2016-06-21 | Class III | Device Design | Revision rate trends from within the MicroPort Orthopedics Inc. database evaluated for the modular head Metal on Metal THA systems show an increasing overall trend from 2009 to present and it was found that there was a specific hazard/harm | 68,199 units | 2017-07-01 |
| 2016-06-21 | Class III | Device Design | Revision rate trends from within the MicroPort Orthopedics Inc. database evaluated for the modular head Metal on Metal THA systems show an increasing overall trend from 2009 to present and it was found that there was a specific hazard/harm | 22 units | 2017-07-01 |
| 2016-06-21 | Class III | Device Design | Revision rate trends from within the MicroPort Orthopedics Inc. database evaluated for the modular head Metal on Metal THA systems show an increasing overall trend from 2009 to present and it was found that there was a specific hazard/harm | 500 units | 2017-07-01 |
| 2016-06-21 | Class III | Device Design | Revision rate trends from within the MicroPort Orthopedics Inc. database evaluated for the modular head Metal on Metal THA systems show an increasing overall trend from 2009 to present and it was found that there was a specific hazard/harm | 6,250 units | 2017-07-01 |
| 2016-06-21 | Class III | Device Design | Revision rate trends from within the MicroPort Orthopedics Inc. database evaluated for the modular head Metal on Metal THA systems show an increasing overall trend from 2009 to present and it was found that there was a specific hazard/harm | 5,009 units | 2017-07-01 |
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.