Redapt
REDAPT 0 Degree Cemented Screw In Trial Liner 40MM X 62MM
Who Else Makes It
Concentrated in Jiangsu (7), 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 |
| Paragon Medical Device (Changzhou) Co., Ltd. | Changzhou | Jiangsu | Contract manufacturer | 53 |
| Canwell Medical Co., Ltd. | Jinhua | Zhejiang | Contract manufacturer | 42 |
| Suzhou Elite Precision Machinery Co., Ltd. | Kunshan | Jiangsu | Contract manufacturer | 35 |
| Guangzhou Aquila Precise Tools Limited | Guangzhou | Guangdong | Contract manufacturer | 28 |
| 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 |
| 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 14. All 14 manufacturers in China registered for Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
Record
| Listed by | Smith & Nephew, Inc., United States |
|---|---|
| FDA product code | LPH |
| Device type | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented |
| Device class | Class 2 |
| Regulation | 21 CFR 888.3358 |
| Establishment | Contract manufacturer, Remanufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter |
| 510(k) | K150790 |
| Record published | 2016-04-19 |
| Record revised | 2025-07-28 (version 9) |
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 |
| Latex | Labelled latex-free |
| Label carries | lot or batch number, expiry date |
| Storage | Special storage condition: : – |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 71354557 | In distribution | |
| 71354643 | In distribution | |
| 71354422 | In distribution | |
| 71352376 | In distribution | |
| 71354541 | In distribution | |
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| 71354447 | In distribution | |
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| 71354439 | In distribution | |
| 71354441 | In distribution | |
| 71354678 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Initia Total Hip System | Kyocera Medical Technologies, Inc. | 1,000 |
| DJO Surgical | Encore Medical, L.P. | 624 |
| Pinnacle | Depuy Orthopaedics, Inc. | 613 |
| Trilogy® Longevity® | Zimmer, Inc. | 564 |
| Instrument | Howmedica Osteonics Corp | 369 |
| InSitu Hip System | Nextstep Arthropedix | 368 |
| Trilogy® | Zimmer, Inc. | 359 |
| Kyocera Medical Technologies, Inc. | Kyocera Medical Technologies, Inc. | 298 |
| Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented | Zimmer, Inc. | 286 |
| Bencox Hip System | Corentec Co., Ltd. | 286 |
| OrthoMedFlex | Orthomedflex LLC | 257 |
| Sterizo Total Hip System | CPM Medical Consultants, LLC. | 240 |
Showing 12 of 792. All products under Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K242375 | 2024-10-07 |
| K232667 | 2023-10-27 |
| K220959 | 2022-08-18 |
| K211176 | 2022-07-01 |
| K211330 | 2022-01-19 |
| K191002 | 2019-10-31 |
| K190847 | 2019-10-25 |
| K182109 | 2018-11-16 |
| K181366 | 2018-09-24 |
| K171934 | 2017-11-30 |
| K171073 | 2017-11-21 |
| K172684 | 2017-10-03 |
| K150790 | 2015-11-16 |
| K123012 | 2012-10-24 |
| K122244 | 2012-08-23 |
| K110135 | 2011-10-14 |
| K103256 | 2011-01-31 |
| K092098 | 2010-01-22 |
| K081566 | 2008-08-21 |
| K072817 | 2008-05-15 |
| K080625 | 2008-05-08 |
| K072417 | 2008-01-10 |
| K071160 | 2007-10-05 |
| K060630 | 2006-06-14 |
| K022902 | 2002-10-02 |
| K022556 | 2002-08-28 |
| K012787 | 2002-03-15 |
| K013658 | 2001-12-05 |
| K002747 | 2000-12-15 |
| K991026 | 1999-10-22 |
| K991485 | 1999-07-12 |
| K983834 | 1999-02-24 |
Recalls
3 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.
| Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|
| 2019-02-19 | Class II | Packaging process control | Complaints were received indicating that the outer label incorrectly identified the product as size “1” instead of “-1”. The product contained within the package is size “-1” | 58 units | 2021-05-21 |
| 2019-02-19 | Class II | Packaging process control | Complaints were received indicating that the outer label incorrectly identified the product as size “1” instead of “-1”. The product contained within the package is size “-1” | 9 units | 2021-05-21 |
| 2013-11-25 | Class II | Other | One batch of the Reflection(TM) Polyethylene Acetabular Liners may be out of tolerance causing the liner not to fully seat into the shell. | 38 units | 2017-02-01 |
| 2008-11-21 | Not classified | Process control | Liners measuring 28 mm ID and were mismarked as 32 mm. | 19 units | 2011-11-21 |
PMA Approvals
A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.
| PMA number | Decision | Trade name | Approved to |
|---|---|---|---|
| P880025 | 1991-12-04 | AML(R) POROCOAT(R) ACETABULAR CUP PROSTHESIS | Depuy Intl., Ltd. |
| P880076 | 1991-06-17 | WHITESIDE EPS(TM) FEMORAL HIP PROSTHESIS | Dow Corning Wright |
| P850061 | 1991-03-08 | BIAS(R) FIBER METAL TOTAL HIP SYSTEM | Zimmer, Inc. |
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.