Tritanium C

Specialty Tritanium C Inserter With Offset Stop

Registry build 21.09.26
53manufacturers in China registered for this device type
68catalogue numbers in this listing
2510(k) clearances naming this product code
3recalls 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 Tritanium C
Listed by Stryker GmbH, Switzerland
FDA product code LXH
Device type Orthopedic Manual Surgical Instrument
Device class Class 1
Regulation 21 CFR 888.4540
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer
Premarket notification Exempt
Record published 2017-09-18
Record revised 2022-09-16 (version 7)

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, manufacturing date
Sizes Angle 0 to 10 °; length 12 to 14 mm; width 14 to 17 mm; height 4 to 10 mm
Distribution end date 2024-07-04
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Tritanium C
Catalogue number Size Status
48981207 Angle 10.0 ° In distribution
48980509 Length 14.0 mm In distribution
48986705 Width 17.0 mm In distribution
48981509 Height 9.0 mm In distribution
48981505 Height 5.0 mm In distribution
48980207 Height 7.0 mm In distribution
48981507 Length 14.0 mm In distribution
48980710 Width 17.0 mm In distribution
IS4419TRC In distribution
48980508 Height 8.0 mm In distribution
48986205 Width 14.0 mm In distribution
48980015 In distribution
48981506 Height 6.0 mm In distribution
48986708 Angle 6.0 ° In distribution
48980208 Angle 0.0 ° In distribution
48986505 Length 14.0 mm In distribution
48980706 Width 17.0 mm In distribution
48986209 Width 14.0 mm In distribution
48980210 Height 10.0 mm In distribution
48986206 Height 6.0 mm In distribution
48986709 Angle 6.0 ° In distribution
48981705 Width 17.0 mm In distribution
48980506 Angle 0.0 ° In distribution
48986508 Length 14.0 mm In distribution
48981706 Width 17.0 mm In distribution
IS4398TRC In distribution
48980510 Angle 0.0 ° In distribution
48986506 Width 15.0 mm In distribution
48981210 Angle 10.0 ° In distribution
48980705 Angle 0.0 ° In distribution
48986710 Height 10.0 mm In distribution
48981707 Height 7.0 mm In distribution
48980709 Height 9.0 mm In distribution
48986706 Height 6.0 mm In distribution
48981709 Height 9.0 mm In distribution
48981209 Angle 10.0 ° In distribution
48986510 Length 14.0 mm In distribution
48980708 Width 17.0 mm In distribution
48989000 In distribution
48986509 Height 9.0 mm In distribution
48981205 Width 14.0 mm In distribution
48981708 Angle 10.0 ° In distribution
48980209 Width 14.0 mm In distribution
48980014 In distribution
48981206 Width 14.0 mm In distribution
48980505 Width 15.0 mm In distribution
48981510 Height 10.0 mm In distribution
48980001 In distribution
48986707 Angle 6.0 ° In distribution
48986208 Length 12.0 mm In distribution
48986207 Width 14.0 mm In distribution
48981208 Length 12.0 mm In distribution
IS4396TRC02 Width 17.0 mm In distribution
48980206 Length 12.0 mm In distribution
48981710 Length 14.0 mm In distribution
48986210 Angle 6.0 ° In distribution
48980707 Angle 0.0 ° In distribution
48981508 Length 14.0 mm In distribution
48980205 Length 12.0 mm In distribution
IS4534TRC In distribution
48980507 Width 15.0 mm In distribution
IS4396TRC04 Length 14.0 mm In distribution
IS4396TRC03 Height 8.0 mm In distribution
48986507 Height 7.0 mm In distribution
IS4396TRC01 Width 14.0 mm In distribution
IS4392TRC02 Width 17.0 mm Withdrawn
IS4392TRC01 Length 12.0 mm Withdrawn
IS4392TRC03 Width 17.0 mm 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

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K941605 1994-08-05
K843942 1985-04-15

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
2025-03-28 Class II Device Design The metal ring at the end of the Guide Wire with Ruler Tube may detach from the main body of the instrument during use in surgery. 1588 units
2025-03-28 Class II Device Design The metal ring at the end of the Guide Wire with Ruler Tube may detach from the main body of the instrument during use in surgery. 6407 units
2017-11-09 Class II Environmental control Lack of sterility assurance as bioburden levels were found to be higher than internal acceptable rates. 320 2019-04-16

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