Truliant CC
Truliant Femoral Offset Bushing Guide Adapter, Size 3
Who Else Makes It
Concentrated in Jiangsu (10), Shanghai (4), Beijing (3). 13 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 |
| B-ONE Medical (Suzhou) Co., Ltd. | Suzhou | Jiangsu | Contract manufacturer | 23 |
| LX Precision Shanghai Co Ltd | Shanghai | Shanghai | Contract manufacturer | 19 |
| Stryker (Suzhou) Medical Technology Co., Ltd. | Suzhou | Jiangsu | Contract manufacturer | 19 |
| Stryker Orthmed (Changzhou) Medical Instrument Co., Ltd. | Changzhou | Jiangsu | Contract manufacturer | 10 |
| b-ONE Medical (Beijing) Co., Ltd. | Beijing | Beijing | Contract manufacturer | 7 |
| Changzhou Wastonortho Medical Appliance Co., Ltd. | Changzhou | Jiangsu | Contract manufacturer | 5 |
Showing 12 of 21. All 21 manufacturers in China registered for Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Record
| Listed by | Exactech, Inc., United States |
|---|---|
| FDA product code | JWH |
| Device type | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer |
| Device class | Class 2 |
| Regulation | 21 CFR 888.3560 |
| Establishment | Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter |
| 510(k) | K150890 |
| Record published | 2023-11-09 |
| Record revised | 2024-09-11 (version 2) |
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, serial number |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 02-012-65-3019 | In distribution | |
| 02-011-06-0740 | In distribution | |
| 02-012-65-5019 | In distribution | |
| 02-013-60-1080 | In distribution | |
| 02-012-65-4021 | In distribution | |
| 02-013-60-2216 | In distribution | |
| 02-019-50-0330 | In distribution | |
| 02-013-60-1180 | In distribution | |
| 02-012-60-1080 | In distribution | |
| 02-012-65-9217 | In distribution | |
| 02-013-60-1016 | In distribution | |
| 02-010-06-0220 | In distribution | |
| 02-012-60-2020 | In distribution | |
| 02-012-60-1416 | In distribution | |
| 02-012-50-5011 | In distribution | |
| 02-019-10-0210 | In distribution | |
| 02-010-06-0532 | In distribution | |
| 02-012-65-1021 | In distribution | |
| 02-010-06-0250 | In distribution | |
| 02-010-06-0512 | In distribution | |
| 02-019-30-0111 | In distribution | |
| 02-012-65-3025 | In distribution | |
| 02-013-60-2480 | In distribution | |
| 02-011-06-0610 | In distribution | |
| 02-013-60-1425 | In distribution | |
| 02-019-30-0202 | In distribution | |
| 02-013-61-4000 | In distribution | |
| 02-012-65-4009 | In distribution | |
| 02-011-06-0401 | In distribution | |
| 02-012-50-2511 | In distribution | |
| 02-012-65-1015 | In distribution | |
| 02-012-60-1220 | In distribution | |
| 02-013-60-2280 | In distribution | |
| 02-013-60-1680 | In distribution | |
| 02-012-50-2011 | In distribution | |
| 02-010-06-0350 | In distribution | |
| 02-012-65-2021 | In distribution | |
| 02-013-60-1512 | In distribution | |
| 02-012-50-4513 | In distribution | |
| 02-013-50-1511 | In distribution | |
| 02-012-60-1020 | In distribution | |
| 02-012-65-4015 | In distribution | |
| 02-012-65-3021 | In distribution | |
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| 02-013-61-6000 | In distribution | |
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| 02-019-50-0004 | In distribution | |
| 02-012-65-9325 | In distribution | |
| 02-013-60-1816 | In distribution | |
| 02-012-65-2011 | In distribution | |
| 02-012-65-3011 | In distribution | |
| 02-013-50-3512 | In distribution | |
| 02-011-06-0720 | In distribution | |
| 02-012-61-6000 | In distribution | |
| 02-011-06-0650 | In distribution | |
| 02-013-50-1512 | In distribution | |
| 02-010-06-0542 | In distribution | |
| 02-012-65-5029 | In distribution | |
| 02-012-65-5025 | In distribution | |
| 02-012-50-1511 | In distribution | |
| 02-012-60-2412 | In distribution | |
| 02-019-30-0112 | In distribution | |
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| 02-013-60-1440 | In distribution | |
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| 02-019-30-0122 | In distribution | |
| 02-012-65-9313 | In distribution | |
| 02-019-30-0120 | In distribution | |
| 02-011-07-2510 | In distribution | |
| 02-019-50-0320 | In distribution | |
| 02-012-65-4025 | In distribution | |
| 02-019-30-0201 | In distribution | |
| 02-019-30-0303 | In distribution | |
| 02-012-50-3511 | In distribution | |
| 02-012-50-3514 | In distribution | |
| 02-012-60-1280 | In distribution | |
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| 02-012-60-2420 | In distribution | |
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| 02-012-50-3013 | In distribution | |
| 02-012-65-9229 | In distribution | |
| 02-012-60-2216 | In distribution | |
| 02-013-60-1216 | In distribution | |
| 02-019-30-0203 | In distribution |
Showing 250 of 300 catalogue numbers.
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Prophecy® | Microport Orthopedics Inc. | 4,423 |
| Exult Knee Replacement System | Corentec Co., Ltd. | 1,770 |
| Freedom | Maxx Orthopedics Inc. | 1,693 |
| Legion | Smith & Nephew, Inc. | 1,534 |
| MyKnee | Medacta International SA | 1,466 |
| Journey | Smith & Nephew, Inc. | 1,339 |
| Persona® | Zimmer, Inc. | 1,254 |
| DJO Surgical | Encore Medical, L.P. | 1,131 |
| U2 Total Knee System | United Orthopedic Corp. | 1,078 |
| CKS Plus | Shalby Advanced Technologies, Inc. | 1,024 |
| Lospa Modular Knee System | Corentec Co., Ltd. | 1,020 |
| Natural-Knee® | Zimmer, Inc. | 980 |
Showing 12 of 1,175. All products under Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K223252 | 2023-07-17 |
| K171045 | 2017-04-28 |
| K170240 | 2017-02-23 |
| K153595 | 2016-03-25 |
| K160484 | 2016-03-18 |
| K152170 | 2015-09-03 |
| K150890 | 2015-05-29 |
| K132161 | 2013-10-11 |
| K123687 | 2013-03-20 |
| K123342 | 2013-01-10 |
| K121307 | 2012-05-31 |
| K111400 | 2011-07-28 |
| K101981 | 2010-08-02 |
| K093360 | 2010-01-11 |
| K082022 | 2008-09-02 |
| K071738 | 2007-08-15 |
| K032522 | 2004-05-28 |
| K033883 | 2004-02-13 |
| K032606 | 2003-09-23 |
| K030686 | 2003-04-02 |
| K023186 | 2002-10-17 |
| K012251 | 2001-07-31 |
| K011976 | 2001-07-16 |
| K010434 | 2001-03-13 |
| K954208 | 1996-02-26 |
| K933494 | 1995-03-10 |
| K932690 | 1995-02-09 |
| K933610 | 1995-01-17 |
| K935773 | 1994-12-09 |
| K932776 | 1994-10-20 |
| K935726 | 1994-10-20 |
| K936079 | 1994-09-07 |
Recalls Naming This Product
4 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 |
|---|---|---|---|---|---|---|---|
| Exactech, Inc. | 510(k) number | 2023-11-21 | Class II | Packaging change control | Exactech has received 3 complaints for 4 devices related to a loss of vacuum in the inner-most vacuum bag. | ||
| Exactech, Inc. | 510(k) number | 2020-01-27 | Class II | Labeling mix-ups | These Truliant Splined Stem Extension, 18mm x 120mm were found to have a labeling error. The upper right corner of the label incorrectly identifies the implant size as 17mm x 80mm when the implant size is 18mm x 120mm. | 4 units | |
| Exactech, Inc. | 510(k) number | 2018-05-08 | Class II | Under Investigation by firm | Potentially have non-conforming internal threads. | 1 | |
| Exactech, Inc. | 510(k) number | 2017-04-07 | Class II | Process control | Missing Screw in carton. Nine (9) serial numbers were identified as being inadvertently packaged as one per carton when two per carton are required. | 9 devices | 2020-08-04 |
Recalls
37 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 |
|---|---|---|---|---|---|
| 2024-04-18 | Class II | Under Investigation by firm | Exactech is recalling all affected UHMWPE (ultra-high molecular weight polyethylene) knee patella components packaged in out of specification vacuum bags. | ||
| 2024-04-18 | Class II | Under Investigation by firm | Exactech is recalling all affected UHMWPE (ultra-high molecular weight polyethylene) knee patella components packaged in out of specification vacuum bags. | ||
| 2024-04-18 | Class II | Under Investigation by firm | Exactech is recalling all affected UHMWPE (ultra-high molecular weight polyethylene) knee patella components packaged in out of specification vacuum bags. | ||
| 2024-04-18 | Class II | Under Investigation by firm | Exactech is recalling all affected UHMWPE (ultra-high molecular weight polyethylene) knee patella components packaged in out of specification vacuum bags. | ||
| 2023-11-21 | Class II | Packaging change control | Exactech has received 3 complaints for 4 devices related to a loss of vacuum in the inner-most vacuum bag. | ||
| 2023-11-21 | Class II | Packaging change control | Exactech has received 3 complaints for 4 devices related to a loss of vacuum in the inner-most vacuum bag. | ||
| 2023-11-21 | Class II | Packaging change control | Exactech has received 3 complaints for 4 devices related to a loss of vacuum in the inner-most vacuum bag. | ||
| 2023-11-21 | Class II | Packaging change control | Exactech has received 3 complaints for 4 devices related to a loss of vacuum in the inner-most vacuum bag. | ||
| 2021-08-30 | Class II | Process control | Inserts were packaged in vacuum bags that lacked an additional oxygen barrier layer. | 33,103 devices | |
| 2021-08-30 | Class II | Process control | Inserts were packaged in vacuum bags that lacked an additional oxygen barrier layer. | 242,397 devices | |
| 2021-08-30 | Class II | Process control | Inserts were packaged in vacuum bags that lacked an additional oxygen barrier layer. | 12 devices | |
| 2021-08-30 | Class II | Process control | Inserts were packaged in vacuum bags that lacked an additional oxygen barrier layer. | 31,201 devices | |
| 2021-08-30 | Class II | Process control | Inserts were packaged in vacuum bags that lacked an additional oxygen barrier layer. | 109,787 devices | |
| 2021-08-30 | Class II | Process control | Inserts were packaged in vacuum bags that lacked an additional oxygen barrier layer. | 8,985 devices | |
| 2021-08-30 | Class II | Process control | Inserts were packaged in vacuum bags that lacked an additional oxygen barrier layer. | 41 devices | |
| 2019-03-13 | Class II | Under Investigation by firm | 2.5 Truliant Fit Trays were mismarked as 3 | 18 units | 2021-04-22 |
| 2017-09-19 | Class II | Labeling design | There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. | 665 devices | 2021-06-21 |
| 2017-09-19 | Class II | Labeling design | There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. | 801 devices | 2021-06-21 |
| 2017-09-19 | Class II | Labeling design | There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. | 198 devices | 2021-06-21 |
| 2017-09-19 | Class II | Labeling design | There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. | 678 devices | 2021-06-21 |
| 2017-09-19 | Class II | Labeling design | There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. | 411 devices | 2021-06-21 |
| 2017-09-19 | Class II | Labeling design | There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. | 889 devices | 2021-06-21 |
| 2017-09-19 | Class II | Labeling design | There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. | 606 devices | 2021-06-21 |
| 2017-09-19 | Class II | Labeling design | There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. | 311 devices | 2021-06-21 |
| 2017-09-19 | Class II | Labeling design | There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. | 386 devices | 2021-06-21 |
| 2017-09-19 | Class II | Labeling design | There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. | 333 devices | 2021-06-21 |
| 2017-09-19 | Class II | Labeling design | There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. | 733 devices | 2021-06-21 |
| 2017-09-19 | Class II | Labeling design | There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. | 207 devices | 2021-06-21 |
| 2017-09-19 | Class II | Labeling design | There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. | 527 devices | 2021-06-21 |
| 2017-09-19 | Class II | Labeling design | There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. | 575 devices | 2021-06-21 |
| 2017-09-19 | Class II | Labeling design | There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. | 643 devices | 2021-06-21 |
| 2017-09-19 | Class II | Labeling design | There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. | 109 devices | 2021-06-21 |
| 2017-09-19 | Class II | Labeling design | There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. | 547 devices | 2021-06-21 |
| 2017-09-19 | Class II | Labeling design | There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. | 656 devices | 2021-06-21 |
| 2017-09-19 | Class II | Labeling design | There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. | 953 devices | 2021-06-21 |
| 2017-09-19 | Class II | Labeling design | There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. | 893 devices | 2021-06-21 |
| 2017-09-19 | Class II | Labeling design | There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray. | 114 devices | 2021-06-21 |
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.