Evos

Evos Large Targeter 4.7MM Cannulated Driver Shaft W/Hall-Jacobs

Registry build 21.09.26
53manufacturers in China registered for this device type
130catalogue numbers in this listing
1510(k) clearance
40recalls on this code

Who Else Makes It

Concentrated in Jiangsu (24), Guangdong (7), Zhejiang (6). 29 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code LXH
Manufacturer City Province Registered as Device types
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
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
B.Braun Medical (Suzhou) Co,.Ltd Suzhou Jiangsu Contract manufacturer 37
Suzhou Elite Precision Machinery Co., Ltd. Kunshan Jiangsu Contract manufacturer 35
Xinhua Healthcare Industry Co., Limited Zibo Shandong Contract manufacturer 30
Guangzhou Aquila Precise Tools Limited Guangzhou Guangdong Contract manufacturer 28
B-ONE Medical (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 23
Suzhou Jinsheng Plastic Co., Ltd. Suzhou Jiangsu Contract manufacturer 23
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Suzhou Ahno Medical Devices Co., Ltd. Suzhou Jiangsu Contract manufacturer 17

Showing 12 of 53. All 53 manufacturers in China registered for Orthopedic Manual Surgical Instrument

Record

Regulatory record for Evos
Listed by Smith & Nephew, Inc., United States
FDA product code LXH
Device type Orthopedic Manual Surgical Instrument
Device class Class 1
Regulation 21 CFR 888.4540
Establishment Contract manufacturer, Remanufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Premarket notification Exempt
Record published 2025-11-12
Record revised 2024-06-05 (version 5)

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
Packaging Box of 6
Sizes Length 82 to 460 mm; angle 3 to 30 °
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Evos
Catalogue number Size Status
71175163 Length 460 mm In distribution
71177743 In distribution
71175603 In distribution
71175666 In distribution
71177724 In distribution
71177741 In distribution
71175614 In distribution
71173556 In distribution
71177665 In distribution
71175033 In distribution
71175665 In distribution
71175679 In distribution
71174929 In distribution
71177673 In distribution
71177584 Diameter: 15 mm In distribution
71174916 In distribution
71175165 Length 460 mm In distribution
71175164 Length 360 mm In distribution
71176414 Length: SHORT In distribution
71175031 In distribution
71177737 In distribution
71175627 In distribution
71175625 In distribution
71177760 In distribution
71177047 In distribution
71177730 In distribution
71176690 Diameter: 2.5 mm In distribution
71175637 In distribution
71175141 Angle 3 ° In distribution
71174969 In distribution
71177048 In distribution
71175605 In distribution
71174915 In distribution
71175162 Length 360 mm In distribution
71175034 In distribution
71175140 Angle 3 ° In distribution
71175160 Length 360 mm In distribution
71175681 In distribution
71170186 In distribution
71177721 In distribution
71177757 In distribution
71175082 In distribution
71175609 In distribution
71175144 Diameter: 2.0 mm In distribution
71177727 In distribution
71175092 In distribution
71177765 In distribution
71177043 In distribution
71177008 In distribution
71177020 In distribution
71175095 In distribution
71175619 In distribution
71177692 In distribution
71175093 In distribution
71177045 In distribution
71175090 In distribution
71175646 In distribution
71175638 In distribution
71175612 In distribution
71173306 In distribution
71177735 In distribution
71176002 In distribution
71177694 In distribution
71177761 In distribution
71177722 In distribution
71175663 In distribution
71177726 In distribution
71175689 In distribution
71175642 In distribution
71175641 In distribution
71175620 In distribution
71175611 In distribution
71175167 Length 460 mm In distribution
71177562 In distribution
71177719 In distribution
71176415 Length: LONG In distribution
71175602 In distribution
71175601 In distribution
71175091 In distribution
71175616 In distribution
71177725 In distribution
71175610 In distribution
71177749 In distribution
71177733 In distribution
71175147 Diameter: 2.5 mm In distribution
71177561 In distribution
71175615 In distribution
71177718 In distribution
71175036 In distribution
71176692 Diameter: 2.5 mm In distribution
71175099 In distribution
71175177 Diameter: 2.0 mm In distribution
71176693 Diameter: 2.5 mm In distribution
71175626 In distribution
71176416 Angle 30 ° In distribution
E0018058-3 In distribution
71175604 In distribution
71177039 In distribution
71175148 Length 82 mm In distribution
71175690 In distribution
71175647 In distribution
71177745 In distribution
71177728 In distribution
71175618 In distribution
71177019 In distribution
71177021 In distribution
71175146 Size: THREAD LENGTH 20MM In distribution
71175600 In distribution
71177740 In distribution
71175094 In distribution
71176633 In distribution
71175639 In distribution
71177752 In distribution
71175161 Diameter: 2.5 mm In distribution
71175035 In distribution
71177746 In distribution
71175633 In distribution
71177672 In distribution
71176003 In distribution
71175678 Diameter: 25 mm In distribution
71177046 In distribution
71177762 In distribution
71177007 In distribution
71175166 Diameter: 3.2 mm In distribution
71175636 In distribution
71177759 In distribution
71175606 In distribution
71175662 In distribution
71176694 Diameter: 3.2 mm In distribution
71175143 Angle: 2 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Razek Equipamentos Razek Equipamentos Ltda 11,578
Orthopedic Manual Surgical Instrument Globus Medical, Inc. 4,784
Instrument Howmedica Osteonics Corp 4,539
Orthopedic Manual Surgical Instrument Ortho Development Corp. 4,076
Knee Instruments Medacta International SA 3,944
Kyocera Medical Technologies, Inc. Kyocera Medical Technologies, Inc. 3,420
Arthrex® Arthrex, Inc. 3,106
Spine Instruments Medacta International SA 2,892
Orthopedic Manual Surgical Instrument Medtronic Sofamor Danek, Inc. 2,766
Hip Instruments Medacta International SA 1,904
Medtronic Reusable Instruments Medtronic Sofamor Danek, Inc. 1,756
ReLine Nuvasive, Inc. 1,208

Showing 12 of 9,501. All products under Orthopedic Manual Surgical Instrument

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K001507 2000-06-14

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.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2020-06-29 Class II Process design The 4.5MM PeriLoc Targeter right hand part was anodized green and was marked as a left-hand part. 3 units 2022-02-18
2019-10-07 Class II Process control LAG SCREW 3.2 GUIDE PIN SLEEVE are being recalled due to a manufacturing error. The detent balls in the guide pin sleeve were not drilled to the correct depth, which will cause them to not fully compress. 116 devices 2023-03-08
2019-01-07 Class II Process control The pin that holds the spring mechanism is not properly mounted. The pin could potentially disassemble. 72 units 2020-09-17
2012-04-13 Not classified Packaging Plastic trays which encase these products have burrs on the hinged packaging which can puncture the single barrier sterile pouch, voiding sterility. 927 units 2015-09-22
2012-04-13 Not classified Packaging Plastic trays which encase these products have burrs on the hinged packaging which can puncture the single barrier sterile pouch, voiding sterility. 3435 units 2015-09-22
2012-04-13 Not classified Packaging Plastic trays which encase these products have burrs on the hinged packaging which can puncture the single barrier sterile pouch, voiding sterility. 8195 units 2015-09-22
2012-04-13 Not classified Packaging Plastic trays which encase these products have burrs on the hinged packaging which can puncture the single barrier sterile pouch, voiding sterility. 44 units 2015-09-22
2012-04-13 Not classified Packaging Plastic trays which encase these products have burrs on the hinged packaging which can puncture the single barrier sterile pouch, voiding sterility. 1203 units 2015-09-22
2012-04-13 Not classified Packaging Plastic trays which encase these products have burrs on the hinged packaging which can puncture the single barrier sterile pouch, voiding sterility. 739 units 2015-09-22
2012-04-13 Not classified Packaging Plastic trays which encase these products have burrs on the hinged packaging which can puncture the single barrier sterile pouch, voiding sterility. 867 units 2015-09-22
2012-04-13 Not classified Packaging Plastic trays which encase these products have burrs on the hinged packaging which can puncture the single barrier sterile pouch, voiding sterility. 1434 units 2015-09-22
2012-04-13 Not classified Packaging Plastic trays which encase these products have burrs on the hinged packaging which can puncture the single barrier sterile pouch, voiding sterility. 1300 units 2015-09-22
2012-04-13 Not classified Packaging Plastic trays which encase these products have burrs on the hinged packaging which can puncture the single barrier sterile pouch, voiding sterility. 1693 units 2015-09-22
2011-07-07 Not classified Nonconforming Material/Component Shaft tip (casting) does not meet the SNE 416
specification, which could result in rusting of the Tendon Strippers
570 units 2015-07-23
2010-04-20 Not classified Process control Markings for the drill guides are on the incorrect side: left is printed on right side and right is printed on the left side 12 units 2011-12-07
2009-01-22 Not classified Process design Incorrect depth gauge mark etched onto guide wire pin. Guide pin is too long. 99 units 2011-08-18
2007-07-12 Not classified Packaging process control The carton label may not reflect the correct size of the acetabular cup. 2 units 2010-02-02
2007-07-12 Not classified Packaging process control The carton label may not reflect the correct size of the acetabular cup. 4 units 2010-02-02
2007-07-12 Not classified Packaging process control The carton label may not reflect the correct size of the acetabular cup. 1 unit 2010-02-02
2007-07-12 Not classified Packaging process control The carton label may not reflect the correct size of the acetabular cup. 10 units 2010-02-02
2007-07-12 Not classified Packaging process control The carton label may not reflect the correct size of the acetabular cup. 1 unit 2010-02-02
2007-07-12 Not classified Packaging process control The carton label may not reflect the correct size of the acetabular cup. 8 units 2010-02-02
2007-07-12 Not classified Packaging process control The carton label may not reflect the correct size of the acetabular cup. 21 units 2010-02-02
2007-07-12 Not classified Packaging process control The carton label may not reflect the correct size of the acetabular cup. 1 unit 2010-02-02
2007-07-12 Not classified Packaging process control The carton label may not reflect the correct size of the acetabular cup. 42 units 2010-02-02
2007-07-12 Not classified Packaging process control The carton label may not reflect the correct size of the acetabular cup. 10 units 2010-02-02
2007-07-12 Not classified Packaging process control The carton label may not reflect the correct size of the acetabular cup. 1 unit 2010-02-02
2007-07-12 Not classified Packaging process control The carton label may not reflect the correct size of the acetabular cup. 8 units 2010-02-02
2007-07-12 Not classified Packaging process control The carton label may not reflect the correct size of the acetabular cup. 10 units 2010-02-02
2007-07-12 Not classified Packaging process control The carton label may not reflect the correct size of the acetabular cup. 30 units 2010-02-02
2007-07-12 Not classified Packaging process control The carton label may not reflect the correct size of the acetabular cup. 1 unit 2010-02-02
2007-07-12 Not classified Packaging process control The carton label may not reflect the correct size of the acetabular cup. 6 units 2010-02-02
2007-07-12 Not classified Packaging process control The carton label may not reflect the correct size of the acetabular cup. 12 units 2010-02-02
2007-07-12 Not classified Packaging process control The carton label may not reflect the correct size of the acetabular cup. 9 units 2010-02-02
2007-03-13 Not classified Other The carton label reads BHR Acetabular Cup 60mm contained a 58mm cup. 1 unit 2011-10-28
2007-03-13 Not classified Other The carton label reads BHR Acetabular Cup 60mm contained a 58mm cup. 1 unit 2011-10-28
2007-03-13 Not classified Other The carton label reads BHR Acetabular Cup 60mm contained a 58mm cup. 4 units 2011-10-28
2007-03-13 Not classified Other The carton label reads BHR Acetabular Cup 60mm contained a 58mm cup. 1 unit 2011-10-28
2007-03-13 Not classified Other The carton label reads BHR Acetabular Cup 60mm contained a 58mm cup. 1 unit 2011-10-28
2006-08-29 Not classified Other Tibial punches were not manufactured to specification and could break at the tip during use. 4800 units 2010-04-12

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