Truliant CC

Truliant Femoral Offset Bushing Guide Adapter, Size 3

Registry build 21.09.26
21manufacturers in China registered for this device type
340catalogue numbers in this listing
32510(k) clearances naming this product code
40recalls on this code

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.

Chinese manufacturers registered for FDA product code JWH
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

Regulatory record for Truliant CC
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

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 numbers for Truliant CC
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
02-012-65-9221 In distribution
02-012-60-2480 In distribution
02-011-06-0592 In distribution
02-012-65-9113 In distribution
02-011-06-0492 In distribution
02-013-50-5012 In distribution
02-011-07-5015 In distribution
02-012-60-1420 In distribution
02-011-06-0402 In distribution
02-013-61-6000 In distribution
02-012-50-4014 In distribution
02-011-06-0730 In distribution
02-011-07-2015 In distribution
02-013-50-4513 In distribution
02-019-30-0004 In distribution
02-012-60-1816 In distribution
02-011-07-5510 In distribution
02-013-50-2513 In distribution
02-019-10-0250 In distribution
02-012-65-9129 In distribution
02-012-65-9315 In distribution
02-010-07-1015 In distribution
02-012-50-4511 In distribution
02-013-60-2012 In distribution
02-013-60-1516 In distribution
02-013-60-1025 In distribution
02-012-65-1029 In distribution
02-012-65-9329 In distribution
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02-012-65-4029 In distribution
02-013-50-1012 In distribution
02-012-50-2013 In distribution
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02-012-65-9125 In distribution
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02-013-50-2013 In distribution
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02-019-10-0240 In distribution
02-012-65-1019 In distribution
02-011-07-4510 In distribution
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02-012-60-1412 In distribution
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02-012-65-9229 In distribution
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02-013-60-1216 In distribution
02-019-30-0203 In distribution

Showing 250 of 300 catalogue numbers.

Same Product Code

Other products under the same FDA 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

FDA 510(k) clearances naming this product code
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.

Recalls naming the identifiers of Truliant CC
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.

Recalls referencing this product code
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.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer