Evos

Evos Pelvic 7.0MM X 110MM Cannulated Screw Partially Threaded 32MM

Registry build 21.09.26
31manufacturers in China registered for this device type
1,051catalogue numbers in this listing
27510(k) clearances naming this product code
36recalls on this code

Who Else Makes It

Concentrated in Jiangsu (15), Shanghai (5), Zhejiang (3). 19 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HWC
Manufacturer City Province Registered as Device types
MicroPort Orthopedics Global Supply Center Limited Shanghai Shanghai Contract manufacturer 82
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
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
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Suzhou Ahno Medical Devices Co., Ltd. Suzhou Jiangsu Contract manufacturer 17
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Sanbor Medical Xiamen, Inc. Xiamen Fujian Contract manufacturer 16
Suzhou Kangli Orthopaedics Instrument Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 11

Showing 12 of 31. All 31 manufacturers in China registered for Screw, Fixation, Bone

Record

Regulatory record for Evos
Listed by Smith & Nephew, Inc., United States
FDA product code HWC
Device type Screw, Fixation, Bone
Device class Class 2
Regulation 21 CFR 888.3040
Establishment Contract manufacturer, Remanufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K241666
Record published 2025-05-22
Record revised 2025-11-20 (version 12)

Specifications

Specifications
MRI safety MR Conditional
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date
Storage Special storage condition: : –
Sizes Length 6 to 170 mm
Distribution end date 2022-03-17
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Evos
Catalogue number Size Status
70976060 60 MM – 32 MM PARTIALLY THREADED: 60 MM – 32 MM PARTIALLY THREADED In distribution
70977110 110 MM – 32 MM PARTIALLY THREADED: 110 MM – 32 MM PARTIALLY THREADED In distribution
72504562N In distribution
70473556 In distribution
72413548 In distribution
70875075 In distribution
70899180 180 MM – 65 MM UNTHREADED: 180 MM – 65 MM UNTHREADED In distribution
72413532N In distribution
72504615N In distribution
72546570N In distribution
72526744N In distribution
70889115 115 MM – 35 MM UNTHREADED: 115 MM – 35 MM UNTHREADED In distribution
72556610 In distribution
70878125 In distribution
70898140 140 MM – 65 MM UNTHREADED: 140 MM – 65 MM UNTHREADED In distribution
70875140 In distribution
70878085 In distribution
72546555 In distribution
72403640 Length 140 mm In distribution
72535744N In distribution
70898180 180 MM – 65 MM UNTHREADED: 180 MM – 65 MM UNTHREADED In distribution
70473546 In distribution
70877105 In distribution
70473570 In distribution
70573580 In distribution
70473532 In distribution
72556585 In distribution
72546590N In distribution
70875100 In distribution
72535748 In distribution
70898145 145 MM – 65 MM UNTHREADED: 145 MM – 65 MM UNTHREADED In distribution
72434795 In distribution
70573522 In distribution
72556570N In distribution
72440614N In distribution
72546580 In distribution
72535815N In distribution
70877065 In distribution
70875080 In distribution
72434734N In distribution
72535810N In distribution
70975085 85 MM – 32 MM PARTIALLY THREADED: 85 MM – 32 MM PARTIALLY THREADED In distribution
72535732N In distribution
70975125 125 MM – 32 MM PARTIALLY THREADED: 125 MM – 32 MM PARTIALLY THREADED In distribution
72504572N In distribution
72504514 In distribution
72535805N In distribution
72556535N In distribution
72413554 Length 54 mm In distribution
72526740N In distribution
72440512 In distribution
72440904N In distribution
72504585N In distribution
70472770 In distribution
70879140 Diameter: 9.0 mm In distribution
72440318 In distribution
72514570 In distribution
70887080 80 MM – 35 MM UNTHREADED: 80 MM – 35 MM UNTHREADED In distribution
70879120 Diameter: 9.0 mm In distribution
70879095 Length 95 mm In distribution
70473595 In distribution
70876075 In distribution
70975120 120 MM – 32 MM PARTIALLY THREADED: 120 MM – 32 MM PARTIALLY THREADED In distribution
70978170 170 MM – 32 MM PARTIALLY THREADED: 170 MM – 32 MM PARTIALLY THREADED In distribution
72556625 In distribution
70879075 In distribution
72535740N In distribution
72535738N In distribution
70887085 85 MM – 35 MM UNTHREADED: 85 MM – 35 MM UNTHREADED In distribution
72413585N In distribution
72514538 In distribution
70472738 In distribution
72504590 In distribution
70573526 In distribution
72514530N In distribution
70473530 In distribution
72441007 In distribution
72504558 In distribution
70978180 180 MM – 32 MM PARTIALLY THREADED: 180 MM – 32 MM PARTIALLY THREADED In distribution
70976075 75 MM – 32 MM PARTIALLY THREADED: 75 MM – 32 MM PARTIALLY THREADED In distribution
70473115 In distribution
72526805 In distribution
72403570 Length 70 mm In distribution
72440507 In distribution
72403546N In distribution
72440918N In distribution
72514630 In distribution
72526722 In distribution
70573590 In distribution
72556620 In distribution
72514548N In distribution
76112050 In distribution
72526780 In distribution
72526736 In distribution
72440802 In distribution
72504528N In distribution
70878180 In distribution
70879080 In distribution
72504572 In distribution
72504554 In distribution
72514412 In distribution
72441010 In distribution
72514544N In distribution
72556560N In distribution
72413575N In distribution
72514520 In distribution
72514412N In distribution
72514566 In distribution
72402756 Diameter: 2.7 mm In distribution
70572756 In distribution
72504524 In distribution
70877150 In distribution
72504558N In distribution
72514518 In distribution
72546545N In distribution
70573538 In distribution
72424716N In distribution
72413513 In distribution
72546565 In distribution
72546550N In distribution
70878090 In distribution
70975080 80 MM – 32 MM PARTIALLY THREADED: 80 MM – 32 MM PARTIALLY THREADED In distribution
72535805 In distribution
72535765 In distribution
72440308 In distribution
72514574 In distribution
72514516N In distribution
70889090 90 MM – 35 MM UNTHREADED: 90 MM – 35 MM UNTHREADED In distribution
70976055 55 MM – 32 MM PARTIALLY THREADED: 55 MM – 32 MM PARTIALLY THREADED In distribution
70889075 75 MM – 35 MM UNTHREADED: 75 MM – 35 MM UNTHREADED In distribution
72514408 In distribution
72413585 Diameter: 3.5 mm In distribution
76112724 In distribution
72403524N In distribution
72514544 In distribution
72403511 Diameter: 3.5 mm In distribution
72514522 In distribution
72514514 In distribution
72440914N In distribution
70898130 130 MM – 65 MM UNTHREADED: 130 MM – 65 MM UNTHREADED In distribution
XT001183-2 In distribution
70876095 In distribution
70473536 In distribution
72535785 In distribution
72556545 In distribution
70877170 In distribution
70978140 140 MM – 32 MM PARTIALLY THREADED: 140 MM – 32 MM PARTIALLY THREADED In distribution
72556570 In distribution
72514568N In distribution
70572738 In distribution
72434732N In distribution
72424714N In distribution
70975100 100 MM – 32 MM PARTIALLY THREADED: 100 MM – 32 MM PARTIALLY THREADED In distribution
72504540 In distribution
72441012 In distribution
72504578 In distribution
72526810 In distribution
72526748 In distribution
72535820N In distribution
72556595 In distribution
72504564 In distribution
70975090 90 MM – 32 MM PARTIALLY THREADED: 90 MM – 32 MM PARTIALLY THREADED In distribution
72526755 In distribution
70573550 In distribution
72546620N In distribution
72546590 In distribution
70473538 In distribution
70978135 135 MM – 32 MM PARTIALLY THREADED: 135 MM – 32 MM PARTIALLY THREADED In distribution
72504544N In distribution
72504610N In distribution
72504538N In distribution
70573560 In distribution
72434795N In distribution
70876175 In distribution
72441004 In distribution
70572732 In distribution
70976125 125 MM – 32 MM PARTIALLY THREADED: 125 MM – 32 MM PARTIALLY THREADED In distribution
70473528 In distribution
70572736 In distribution
70878075 In distribution
72414750 In distribution
72440610N In distribution
70898150 150 MM – 65 MM UNTHREADED: 150 MM – 65 MM UNTHREADED In distribution
70976095 95 MM – 32 MM PARTIALLY THREADED: 95 MM – 32 MM PARTIALLY THREADED In distribution
70976130 130 MM – 32 MM PARTIALLY THREADED: 130 MM – 32 MM PARTIALLY THREADED In distribution
72413540 In distribution
72403590 Diameter: 3.5 mm In distribution
72424805N In distribution
72526810N In distribution
70573558 In distribution
72414720 In distribution
70877180 In distribution
72403511N In distribution
70473542 In distribution
72504600 In distribution
72440622 In distribution
72424800N In distribution
72535765N In distribution
72535770 In distribution
70875085 In distribution
70879170 Length 170 mm In distribution
72535755 In distribution
70573532 In distribution
70472750 In distribution
70878150 In distribution
72504562 In distribution
72424770N In distribution
70472758 In distribution
72440115 In distribution
70888110 110 MM – 35 MM UNTHREADED: 110 MM – 35 MM UNTHREADED In distribution
70572754 In distribution
70896130 130 MM – 65 MM UNTHREADED: 130 MM – 65 MM UNTHREADED In distribution
70573544 In distribution
72504556N In distribution
70976090 90 MM – 32 MM PARTIALLY THREADED: 90 MM – 32 MM PARTIALLY THREADED In distribution
70978130 130 MM – 32 MM PARTIALLY THREADED: 130 MM – 32 MM PARTIALLY THREADED In distribution
72504552 In distribution
70472752 In distribution
72504568N In distribution
72504610 In distribution
72514558 In distribution
70878115 In distribution
72514574N In distribution
70877175 In distribution
70473565 In distribution
70889070 70 MM – 35 MM UNTHREADED: 70 MM – 35 MM UNTHREADED In distribution
XT001183-4 In distribution
70977150 150 MM – 32 MM PARTIALLY THREADED: 150 MM – 32 MM PARTIALLY THREADED In distribution
72504585 In distribution
70473550 In distribution
72546540N In distribution
72403555N In distribution
72424795N In distribution
72413528 Length 28 mm In distribution
72556550 In distribution
70877140 In distribution
72413560N In distribution
72504560 In distribution
72514410 In distribution
72414716 In distribution
72514528N In distribution
72514526 In distribution
72403554 Diameter: 3.5 mm In distribution
72504566 In distribution
72514595N In distribution
70879145 Diameter: 9.0 mm In distribution
72526726N In distribution
72526785 In distribution
70896165 165 MM – 65 MM UNTHREADED: 165 MM – 65 MM UNTHREADED In distribution
70573534 In distribution

Showing 250 of 300 catalogue numbers.

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Screw, Fixation, Bone Synthes Gmbh 3,975
Aptus Medartis Inc. 3,623
Acumed Acumed LLC 3,187
Arthrex® Arthrex, Inc. 2,781
OsteoMed Osteomed 2,764
Screw, Fixation, Bone AAP Implantate AG 2,176
Screw, Fixation, Bone Zimmer, Inc. 1,993
Arix System Bone Screw Jeil Medical Corporation 1,875
Cannulated Screw System + Tyber Medical 1,814
Cannulated Compression Headless Screw Tyber Medical 1,621
Microware Bone Plates and Bone Screws Microware Precision Co., Ltd. 1,601
Anthem Globus Medical, Inc. 1,538

Showing 12 of 5,775. All products under Screw, Fixation, Bone

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K233396 2023-12-21
K133662 2014-05-15
K122596 2012-11-20
K111994 2011-10-11
K100325 2010-05-04
K090656 2009-06-03
K082516 2008-09-17
K073509 2008-03-04
K060736 2006-04-18
K053344 2006-02-23
K051310 2005-07-26
K050226 2005-02-11
K040542 2004-08-19
K040656 2004-05-25
K040331 2004-04-14
K032224 2003-08-08
K031685 2003-07-01
K023021 2002-10-04
K020159 2002-03-26
K002274 2001-03-07
K003599 2001-02-15
K994202 2000-02-25
K992945 1999-11-18
K984320 1999-01-28
K980841 1998-05-20
K965073 1997-02-27
K943539 1994-10-19

Recalls Naming This Product

3 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of Evos
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Smith & Nephew, Inc. 510(k) number 2021-10-25 Class II Error in labeling The labels on the packages of screws were switched. 224 units
Smith & Nephew, Inc. 510(k) number 2020-08-24 Class II Error in labeling Multiple or incorrect expiration dates were provided on the affected designation labels. 71 units 2022-07-11
Smith & Nephew, Inc. 510(k) number 2017-11-29 Class II Employee error One lot of EVOS 2.4MM Flex Plate 6 Hole packaging contained templates. 12 2020-09-01

Recalls

11 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
2025-11-24 Class II Packaging process control Removal of affected lot of screws due to labeling error. 168 units (US 83; OUS 85)
2021-09-20 Class II Process control The product label incorrectly indicated that the screws are fully threaded, but the screws contained in the package were partially threaded. 5 units 2023-03-24
2018-03-07 Class II Under Investigation by firm One lot of D-RAD Self-Taping Locking Screws used with the Distal Radius Fracture Kit were machined out of specification. Screws measured over tolerance within the head thread form by 0.002-0.003 inch. 59 units 2018-10-31
2017-03-09 Class II Labeling Change Control The expiration dates on the labeling are incorrect, the actual expiration dates are before the date on the labeling. 197 units 2019-08-21
2017-03-09 Class II Labeling Change Control The expiration dates on the labeling are incorrect, the actual expiration dates are before the date on the labeling. 100 units 2019-08-21
2017-03-09 Class II Labeling Change Control The expiration dates on the labeling are incorrect, the actual expiration dates are before the date on the labeling. 19 units 2019-08-21
2013-08-06 Class II Packaging Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier. 43385 US 2016-04-20
2013-08-06 Class II Packaging Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier. 24574 US 2016-04-20
2013-08-06 Class II Packaging Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier. 1735 US 2016-04-20
2013-08-06 Class II Packaging Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier. 240 US 2016-04-20
2013-08-06 Class II Packaging Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier. 725 US 2016-04-20
2012-02-06 Not classified Packaging process control Mislabeled: The device was labeled as a standard thread screw (P/N 72201772) on pouch and box,
however the device contained in the packaging is a reverse thread screw (P/N 72201773).
194 units 2016-02-29
2007-08-21 Not classified Nonconforming Material/Component Patient Reaction: Post operative condition sterile fluid pocket has been identified, including the potential for graft failure and premature material degradation. 5530 units 2012-05-09
2007-08-21 Not classified Nonconforming Material/Component Patient Reaction: Post operative condition sterile fluid pocket has been identified, including the potential for graft failure and premature material degradation. 6775 units 2012-05-09
2007-08-21 Not classified Nonconforming Material/Component Patient Reaction: Post operative condition sterile fluid pocket has been identified, including the potential for graft failure and premature material degradation. 1274 units 2012-05-09
2007-08-21 Not classified Nonconforming Material/Component Patient Reaction: Post operative condition sterile fluid pocket has been identified, including the potential for graft failure and premature material degradation. 2375 units 2012-05-09
2007-08-21 Not classified Nonconforming Material/Component Patient Reaction: Post operative condition sterile fluid pocket has been identified, including the potential for graft failure and premature material degradation. 600 units 2012-05-09
2007-08-21 Not classified Nonconforming Material/Component Patient Reaction: Post operative condition sterile fluid pocket has been identified, including the potential for graft failure and premature material degradation. 6925 units 2012-05-09
2007-08-21 Not classified Nonconforming Material/Component Patient Reaction: Post operative condition sterile fluid pocket has been identified, including the potential for graft failure and premature material degradation. 2780 units 2012-05-09
2007-08-21 Not classified Nonconforming Material/Component Patient Reaction: Post operative condition sterile fluid pocket has been identified, including the potential for graft failure and premature material degradation. 1461 units 2012-05-09
2007-08-21 Not classified Nonconforming Material/Component Patient Reaction: Post operative condition sterile fluid pocket has been identified, including the potential for graft failure and premature material degradation. 278 units 2012-05-09
2007-08-21 Not classified Nonconforming Material/Component Patient Reaction: Post operative condition sterile fluid pocket has been identified, including the potential for graft failure and premature material degradation. 2903 units 2012-05-09
2007-08-21 Not classified Nonconforming Material/Component Patient Reaction: Post operative condition sterile fluid pocket has been identified, including the potential for graft failure and premature material degradation. 3251 units 2012-05-09
2007-08-21 Not classified Nonconforming Material/Component Patient Reaction: Post operative condition sterile fluid pocket has been identified, including the potential for graft failure and premature material degradation. 2357 units 2012-05-09
2007-08-21 Not classified Nonconforming Material/Component Patient Reaction: Post operative condition sterile fluid pocket has been identified, including the potential for graft failure and premature material degradation. 1990 units 2012-05-09
2007-08-21 Not classified Nonconforming Material/Component Patient Reaction: Post operative condition sterile fluid pocket has been identified, including the potential for graft failure and premature material degradation. 3001 units 2012-05-09
2007-08-21 Not classified Nonconforming Material/Component Patient Reaction: Post operative condition sterile fluid pocket has been identified, including the potential for graft failure and premature material degradation. 537 units 2012-05-09
2007-08-21 Not classified Nonconforming Material/Component Patient Reaction: Post operative condition sterile fluid pocket has been identified, including the potential for graft failure and premature material degradation. 7805 units 2012-05-09
2007-08-21 Not classified Nonconforming Material/Component Patient Reaction: Post operative condition sterile fluid pocket has been identified, including the potential for graft failure and premature material degradation. 2569 units 2012-05-09
2007-08-21 Not classified Nonconforming Material/Component Patient Reaction: Post operative condition sterile fluid pocket has been identified, including the potential for graft failure and premature material degradation. 275 units 2012-05-09
2007-08-21 Not classified Nonconforming Material/Component Patient Reaction: Post operative condition sterile fluid pocket has been identified, including the potential for graft failure and premature material degradation. 952 units 2012-05-09
2007-08-21 Not classified Nonconforming Material/Component Patient Reaction: Post operative condition sterile fluid pocket has been identified, including the potential for graft failure and premature material degradation. 3791 units 2012-05-09
2007-08-21 Not classified Nonconforming Material/Component Patient Reaction: Post operative condition sterile fluid pocket has been identified, including the potential for graft failure and premature material degradation. 3870 units 2012-05-09
2007-08-21 Not classified Nonconforming Material/Component Patient Reaction: Post operative condition sterile fluid pocket has been identified, including the potential for graft failure and premature material degradation. 4411 units 2012-05-09
2007-08-21 Not classified Nonconforming Material/Component Patient Reaction: Post operative condition sterile fluid pocket has been identified, including the potential for graft failure and premature material degradation. 53 units 2012-05-09
2007-08-21 Not classified Nonconforming Material/Component Patient Reaction: Post operative condition sterile fluid pocket has been identified, including the potential for graft failure and premature material degradation. 500 units 2012-05-09

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