VerSys®

121 catalogue numbers from 7894-17-61, listed by Zimmer, Inc., United States, under Orthopedic Manual Surgical Instrument. 53 manufacturers in China are registered for this product code.

Registry build 21.09.26
53manufacturers in China registered for this device type
121catalogue numbers in this listing
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 VerSys®
Listed by Zimmer, 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, Specification developer, Repacker / relabeller, Manufacturer, Exporter
Premarket notification Exempt
Record published 2016-11-08
Record revised 2020-06-22 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Prescription Prescription only
Label carries lot or batch number, serial number
Sizes Length 190 to 250 mm; outer diameter 9 to 19 mm; height 10 to 30 mm
Distribution end date 2017-05-18

Catalogue Numbers

Catalogue numbers for VerSys®
Catalogue number Size Status
7894-17-61 Size 17 230 mm Stem Length In distribution
7893-22-75 Size 22.5/190 In distribution
7893-15-05 Outer Diameter 15 mm In distribution
7894-24-57 Size 14/15 Extended, 12/14 C-Ring Taper In distribution
7894-16-57 Size 16/17, 12/14 C-Ring Taper In distribution
7896-57 In distribution
7894-02-10 Height 10 mm In distribution
7894-01-30 Size 13/15 In distribution
7890-12-57 Size 12/13 In distribution
7893-13-75 Size 13.5/190 In distribution
7896-24 14 and 15 mm Diameters In distribution
7894-21-81 Length 200 mm In distribution
7893-16-75 Size 16.5/190 In distribution
7894-17-35 Size 17 12/14 C-Ring Taper In distribution
7893-21-24 Size 21.0 X 250 In distribution
7894-16-82 12/14 C-Ring Taper, Size 16.5 In distribution
7894-12-18 Length 190 mm In distribution
7894-22-82 12/14 C-Ring Taper, Size 22.5 In distribution
7894-15-62 Size 15 250 mm Stem Length In distribution
7893-09-05 Outer Diameter 9 mm In distribution
7894-21-82 12/14 C-Ring Taper, Size 21.0 In distribution
7893-11-16 Size 11/150 In distribution
7894-14-57 Size 14/15, 12/14 C-Ring Taper In distribution
7896-53 In distribution
7896-59 In distribution
7894-19-35 Size 19 12/14 C-Ring Taper In distribution
7896-60-04 In distribution
7890-13-60 Size 13 In distribution
7894-13-61 Size 13 210 mm Stem Length In distribution
7894-19-60 Size 19 200 mm Stem Length In distribution
7893-15-24 Size 15.0 X 250 In distribution
7894-15-82 Length 200 mm In distribution
7893-12-16 Size 12/150 In distribution
7890-13-35 Size 13.5 In distribution
7893-22-24 Size 22.5 X 250 In distribution
7893-15-70 Size 15/190 In distribution
7894-13-63 Size 13, 300 mm Stem Length In distribution
7896-60-02 In distribution
7894-11-57 Size 11, 12/14 C-Ring Taper In distribution
7894-13-60 Size 13 170 mm Stem Length In distribution
7893-18-05 Outer Diameter 18 mm In distribution
7893-14-05 Outer Diameter 14 mm In distribution
7894-15-08 Size 15.0, 12/14 C-Ring Taper In distribution
7893-19-05 Outer Diameter 19 mm In distribution
7894-17-60 Size 17 190 mm Stem Length In distribution
7893-18-70 Size 18/190 In distribution
7890-14-57 Size 14/15 In distribution
7896-22 12 and 13 mm Diameters In distribution
7696-61 In distribution
7893-10-05 Outer Diameter 10 mm In distribution
7894-26-57 Size 16 Extended, 12/14 C-Ring Taper In distribution
7894-15-35 Size 15 12/14 C-Ring Taper In distribution
7890-16-57 Size 16/17 In distribution
7894-02-20 Size 17/19 In distribution
7893-12-05 Outer Diameter 12 mm In distribution
7894-13-35 Size 13 12/14 C-Ring Taper In distribution
7890-18-35 Size 18.0/22.5 In distribution
7894-18-82 Length 200 mm In distribution
7894-13-82 Length 200 mm In distribution
7893-13-16 Size 13/150 In distribution
7890-12-35 Size 12.0 In distribution
7896-60-03 In distribution
7893-19-24 Size 19.5 X 250 In distribution
7894-12-57 Size 12/13, 12/14 C-Ring Taper In distribution
7894-19-18 Length 190 mm In distribution
7896-60-01 In distribution
7890-19-60 Size 19 In distribution
7894-19-81 Length 200 mm In distribution
7894-15-81 Length 200 mm In distribution
SSI005079 In distribution
7894-23-57 Size 13 Extended, 12/14 C-Ring Taper In distribution
7894-15-63 Size 15, 300 mm Stem Length In distribution
7894-18-81 Length 200 mm In distribution
7893-13-05 Outer Diameter 13 mm In distribution
7893-18-24 Size 18.0 X 250 In distribution
7894-13-18 Length 190 mm In distribution
7894-13-81 Length 200 mm In distribution
7893-12-70 Size 12/190 In distribution
7894-22-81 12/14 C-Ring Taper, Size 22.5 In distribution
7894-01-20 Size 13/15 In distribution
7896-26 16 and 17 mm Diameters In distribution
7896-20 10 and 11 mm Diameters In distribution
7890-11-57 Size 11 In distribution
7893-21-70 Size 21/190 In distribution
7890-17-60 Size 17 In distribution
7894-15-61 Size 15 220 mm Stem Length In distribution
7890-15-60 Size 15 In distribution
7893-11-05 Outer Diameter 11 mm In distribution
7894-02-30 Height 30 mm In distribution
7894-15-60 Size 15 180 mm Stem Length In distribution
7896-28 18 and 19 mm Diameters In distribution
7894-13-62 Size 13 250 mm Stem Length In distribution
7890-15-35 Size 15.0/16.5 In distribution
7893-19-75 Size 19.5/190 In distribution
7893-16-24 Size 16.5 X 250 In distribution
7893-17-05 Outer Diameter 17 mm In distribution
7893-16-05 Outer Diameter 16 mm In distribution
7894-01-10 Height 10 mm In distribution
7894-19-82 12/14 C-Ring Taper, Size 19.5 In distribution
7894-16-08 Size 16.5, 12/14 C-Ring Taper In distribution
7894-16-81 12/14 C-Ring Taper, Size 16.5 In distribution
7896-18 8 and 9 mm Diameters In distribution
7894-15-11 12/14 C-Ring Taper, Size 15.0 Withdrawn
7894-13-12 12/14 C-Ring Taper, Size 13.5 Withdrawn
7894-19-12 12/14 C-Ring Taper, Size 19.5 Withdrawn
7894-21-11 12/14 C-Ring Taper, Size 21.0 Withdrawn
7894-16-12 12/14 C-Ring Taper, Size 16.5 Withdrawn
7894-15-12 12/14 C-Ring Taper, Size 15.0 Withdrawn
7896-09 Withdrawn
7894-15-13 Size 15.0/16.5 Withdrawn
7894-18-13 Size 18.0/19.5 Withdrawn
7894-22-12 12/14 C-Ring Taper, Size 22.5 Withdrawn
7894-16-11 12/14 C-Ring Taper, Size 16.5 Withdrawn
7894-18-12 12/14 C-Ring Taper, Size 18.0 Withdrawn
7894-21-13 Size 21.0/22.5 Withdrawn
7894-19-11 12/14 C-Ring Taper, Size 19.5 Withdrawn
7894-22-11 Length 250 mm Withdrawn
7894-21-12 12/14 C-Ring Taper, Size 21.0 Withdrawn
7894-18-11 12/14 C-Ring Taper, Size 18.0 Withdrawn
7894-13-11 Length 250 mm Withdrawn
7894-12-13 Size 12.0/13.5 Withdrawn

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

Recalls

40 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
2020-05-05 Class II Under Investigation by firm There are reports of inadequate locking of the extended tab screws. Complaints were reported where the closure top backed out of the screw post-operatively. 3235 total 2022-07-15
2019-10-10 Class II Packaging change control Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration). 5,459,583 total devices 2020-05-19
2019-04-18 Class II Nonconforming Material/Component Incorrect raw material used by the supplier in the manufacturing of the screw component, which could potentially lead to corrosion. 14 units 2020-09-10
2019-04-18 Class II Nonconforming Material/Component Incorrect raw material used by the supplier in the manufacturing of the screw component, which could potentially lead to corrosion. 3 units 2020-09-10
2019-04-18 Class II Nonconforming Material/Component Incorrect raw material used by the supplier in the manufacturing of the screw component, which could potentially lead to corrosion. 41 units 2020-09-10
2019-04-18 Class II Nonconforming Material/Component Incorrect raw material used by the supplier in the manufacturing of the screw component, which could potentially lead to corrosion. 15 2020-09-10
2019-04-18 Class II Nonconforming Material/Component Incorrect raw material used by the supplier in the manufacturing of the screw component, which could potentially lead to corrosion. 10 units 2020-09-10
2019-04-18 Class II Nonconforming Material/Component Incorrect raw material used by the supplier in the manufacturing of the screw component, which could potentially lead to corrosion. 11 units 2020-09-10
2018-10-22 Class II Packaging process control Various Trauma Guide Wires- creases in the sealing area on the end opposite of the product’s chevron opening compromising product sterility 1676 2020-12-30
2018-10-22 Class II Packaging process control Various Trauma Guide Wires- creases in the sealing area on the end opposite of the product’s chevron opening compromising product sterility 4122 2020-12-30
2018-10-22 Class II Packaging process control Various Trauma Guide Wires- creases in the sealing area on the end opposite of the product’s chevron opening compromising product sterility 2080 2020-12-30
2018-10-22 Class II Packaging process control Various Trauma Guide Wires- creases in the sealing area on the end opposite of the product’s chevron opening compromising product sterility 57241 2020-12-30
2018-10-22 Class II Packaging process control Various Trauma Guide Wires- creases in the sealing area on the end opposite of the product’s chevron opening compromising product sterility 9387 2020-12-30
2018-10-22 Class II Packaging process control Various Trauma Guide Wires- creases in the sealing area on the end opposite of the product’s chevron opening compromising product sterility 8027 2020-12-30
2018-10-22 Class II Packaging process control Various Trauma Guide Wires- creases in the sealing area on the end opposite of the product’s chevron opening compromising product sterility 48320 2020-12-30
2018-10-22 Class II Packaging process control Various Trauma Guide Wires- creases in the sealing area on the end opposite of the product’s chevron opening compromising product sterility 12724 2020-12-30
2018-10-22 Class II Packaging process control Various Trauma Guide Wires- creases in the sealing area on the end opposite of the product’s chevron opening compromising product sterility 2519 2020-12-30
2018-10-22 Class II Packaging process control Various Trauma Guide Wires- creases in the sealing area on the end opposite of the product’s chevron opening compromising product sterility 3764 2020-12-30
2018-10-22 Class II Packaging process control Various Trauma Guide Wires- creases in the sealing area on the end opposite of the product’s chevron opening compromising product sterility 780 2020-12-30
2018-10-22 Class II Packaging process control Various Trauma Guide Wires- creases in the sealing area on the end opposite of the product’s chevron opening compromising product sterility 3358 2020-12-30
2018-10-22 Class II Packaging process control Various Trauma Guide Wires- creases in the sealing area on the end opposite of the product’s chevron opening compromising product sterility 48320 2020-12-30
2018-03-26 Class II Under Investigation by firm Potential failure of sterile packaging seal. 19,483 total products 2020-11-18
2018-03-26 Class II Under Investigation by firm Potential failure of sterile packaging seal. 19483 total products 2020-11-18
2018-03-26 Class II Under Investigation by firm Potential failure of sterile packaging seal. 19483 total products 2020-11-18
2018-03-26 Class II Under Investigation by firm Potential failure of sterile packaging seal. 19483 total products 2020-11-18
2018-03-26 Class II Under Investigation by firm Potential failure of sterile packaging seal. 19483 total products 2020-11-18
2018-03-26 Class II Under Investigation by firm Potential failure of sterile packaging seal. 19,483 total products 2020-11-18
2018-03-26 Class II Under Investigation by firm Potential failure of sterile packaging seal. 19,483 total products 2020-11-18
2018-03-26 Class II Under Investigation by firm Potential failure of sterile packaging seal. 19,483 total products 2020-11-18
2017-10-03 Class II Labeling design The Sirus Drill and Flexible Shaft instruments may not be adequately cleaned when utilizing the standard cleaning instructions potentially resulting in infection and subsequent complications. 127 2018-08-20
2017-10-03 Class II Labeling design The Sirus Drill and Flexible Shaft instruments may not be adequately cleaned when utilizing the standard cleaning instructions potentially resulting in infection and subsequent complications. 457 2018-08-20
2017-06-05 Class II Package design/selection The design verification for the previous packaging configuration G928 does not cover the 70cm wires. A design verification has been completed to move the 70cm guide wires to a new packaging configuration. As a result, the products packaged 1,517 units 2019-04-17
2017-06-05 Class II Package design/selection The design verification for the previous packaging configuration G928 does not cover the 70cm wires. A design verification has been completed to move the 70cm guide wires to a new packaging configuration. As a result, the products packaged 7,888 units 2019-04-17
2017-06-05 Class II Package design/selection The design verification for the previous packaging configuration G928 does not cover the 70cm wires. A design verification has been completed to move the 70cm guide wires to a new packaging configuration. As a result, the products packaged 10,116 units 2019-04-17
2017-06-05 Class II Package design/selection The design verification for the previous packaging configuration G928 does not cover the 70cm wires. A design verification has been completed to move the 70cm guide wires to a new packaging configuration. As a result, the products packaged 6,290 units 2019-04-17
2017-06-05 Class II Package design/selection The design verification for the previous packaging configuration G928 does not cover the 70cm wires. A design verification has been completed to move the 70cm guide wires to a new packaging configuration. As a result, the products packaged 1,631 units 2019-04-17
2016-06-27 Class II Under Investigation by firm Zimmer Biomet initiated a voluntary recall of the Twist Drill & V-Tek Twist Drill due to to a potential tolerance stack up identified between the twist drill and the mating Kirschner Wire (K-Wire) component. 169 2017-05-30
2016-06-27 Class II Under Investigation by firm Zimmer Biomet initiated a voluntary recall of the Twist Drill & V-Tek Twist Drill due to to a potential tolerance stack up identified between the twist drill and the mating Kirschner Wire (K-Wire) component. 169 2017-05-30
2016-06-27 Class II Under Investigation by firm Zimmer Biomet initiated a voluntary recall of the Twist Drill & V-Tek Twist Drill due to to a potential tolerance stack up identified between the twist drill and the mating Kirschner Wire (K-Wire) component. 169 2017-05-30
2016-06-27 Class II Under Investigation by firm Zimmer Biomet initiated a voluntary recall of the Twist Drill & V-Tek Twist Drill due to to a potential tolerance stack up identified between the twist drill and the mating Kirschner Wire (K-Wire) component. 169 2017-05-30

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