Reliance LITe

Kerrison Bayoneted Upbiting (Curved UP AT TIP)

Registry build 21.09.26
53manufacturers in China registered for this device type
72catalogue 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 Reliance LITe
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 2019-11-08
Record revised 2024-06-07 (version 6)

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 Height 6 to 16 mm; angle 10 to 90 °; width 2 to 5 mm
Distribution end date 2025-03-17
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Reliance LITe
Catalogue number Size Status
48244102 In distribution
48061200 In distribution
48060814 Height 14.0 mm In distribution
48060816 Height 16.0 mm In distribution
48065500 In distribution
48067000AA In distribution
48244104 In distribution
48060906 Height 6.0 mm In distribution
48244204 In distribution
48242200 Width 2.0 mm In distribution
48241103 In distribution
48060807 Height 7.0 mm In distribution
48242340 Angle 40.0 ° In distribution
48060913 Height 13.0 mm In distribution
48067010AA In distribution
48060808 Height 8.0 mm In distribution
48060916 Height 16.0 mm In distribution
48063201 Angle 30.0 ° In distribution
48060914 Height 14.0 mm In distribution
48060811 Height 11.0 mm In distribution
48242240 Width 2.0 mm In distribution
48067010 In distribution
48062100 In distribution
48245002 In distribution
48060911 Height 11.0 mm In distribution
48060907 Height 7.0 mm In distribution
48063101 Angle 30.0 ° In distribution
48240005 In distribution
48247002 In distribution
48063102 Angle 30.0 ° In distribution
48063200 In distribution
48060813 Height 13.0 mm In distribution
48060408 In distribution
48060909 Height 9.0 mm In distribution
48066104 In distribution
48060810 Height 10.0 mm In distribution
48242390 Width 3.0 mm In distribution
48061001 In distribution
48247001 In distribution
48060912 Height 12.0 mm In distribution
48060401 In distribution
48060809 Height 9.0 mm In distribution
48061101 Angle 30.0 ° In distribution
48063202 Angle 30.0 ° In distribution
48063110 Angle 10.0 ° In distribution
48062101 Angle 30.0 ° In distribution
48244202 In distribution
48060200 In distribution
48060806 Height 6.0 mm In distribution
48066007 Diameter: 3.33 Millimeter In distribution
48242400 Width 4.0 mm In distribution
48066204 In distribution
48063100 In distribution
48242590 Width 5.0 mm In distribution
48061000 In distribution
48060812 Height 12.0 mm In distribution
48060815 Height 15.0 mm In distribution
48065000 In distribution
48061210 Angle 10.0 ° In distribution
48245001 In distribution
48067000 In distribution
48061100 In distribution
48060910 Height 10.0 mm In distribution
48062200 In distribution
48242440 Angle 40.0 ° In distribution
48242490 Width 4.0 mm In distribution
48242290 Angle 90.0 ° In distribution
48060915 Height 15.0 mm In distribution
48067000AB In distribution
48242540 Width 5.0 mm In distribution
48060908 Height 8.0 mm In distribution
48245010 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