Radius

Specialty Sharp, Curved Probe W/Large Gearshift Handle

Registry build 21.09.26
53manufacturers in China registered for this device type
97catalogue 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 Radius
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 2019-11-20
Record revised 2024-12-31 (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 Width 4.5 mm
Distribution end date 2025-01-30
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Radius
Catalogue number Size Status
486619400 In distribution
486619240 In distribution
486619480 In distribution
486619460 In distribution
486619170 In distribution
486619175 In distribution
IS4153RAD In distribution
486619235 In distribution
IS2749RAD In distribution
486619185 In distribution
IS4002RAD In distribution
IS3111SDI In distribution
486619260 In distribution
486619250 In distribution
486619430 In distribution
486619100 In distribution
IS2325RAD In distribution
486619110 In distribution
IS4034RAD In distribution
IS3056RAD In distribution
486619470 In distribution
486619481 In distribution
486619410 In distribution
IS4025RAD Width 4.5 mm In distribution
486619245 In distribution
486619420 In distribution
486619280 In distribution
486619255 In distribution
486619095 In distribution
IS2193RAD Diameter: 7.25 Millimeter In distribution
IS3061RAD In distribution
486619450 In distribution
IS3012RAD In distribution
486619035 Withdrawn
486619385 Withdrawn
486619445 Withdrawn
486619220 Withdrawn
486619190 Withdrawn
486619251 Withdrawn
486619186 Withdrawn
486619130 Withdrawn
486619370 Withdrawn
486619046 Diameter: 1.3 Millimeter Withdrawn
486619055 Diameter: 4.75 Millimeter Withdrawn
486619001 Withdrawn
486619030 Withdrawn
486619350 Diameter: 5.75 Millimeter Withdrawn
486619065 Withdrawn
486619061 Diameter: 6.75 Millimeter Withdrawn
486619080 Withdrawn
486619000 Withdrawn
486619390 Withdrawn
486619085 Withdrawn
486619090 Withdrawn
486619025 Withdrawn
486619160 Diameter: 4.5 Millimeter Withdrawn
486619210 Withdrawn
486619058 Diameter: 7.75 Millimeter Withdrawn
486619125 Withdrawn
486619052 Diameter: 4.0 Millimeter Withdrawn
486619050 Withdrawn
486619002 Withdrawn
486619355 Diameter: 6.75 Millimeter Withdrawn
486619043 Withdrawn
486619020 Withdrawn
486619320 Diameter: 9.75 Millimeter Withdrawn
486619180 Withdrawn
486619265 Withdrawn
486619056 Diameter: 5.75 Millimeter Withdrawn
486619070 Withdrawn
486619120 Diameter: 3.5 Millimeter Withdrawn
486619155 Withdrawn
486619054 Withdrawn
486619165 Withdrawn
486619005 Withdrawn
486619138 Withdrawn
486619380 Withdrawn
486619145 Withdrawn
486619166 Withdrawn
486619270 Withdrawn
486619062 Diameter: 7.75 Millimeter Withdrawn
486619315 Diameter: 8.75 Millimeter Withdrawn
486619135 Withdrawn
486619041 Withdrawn
486619345 Withdrawn
486619150 Withdrawn
486619075 Withdrawn
486619010 Withdrawn
486619051 Diameter: 9.75 Millimeter Withdrawn
486619057 Diameter: 6.75 Millimeter Withdrawn
486619215 Withdrawn
486619040 Withdrawn
486619045 Diameter: 1.3 Millimeter Withdrawn
486619440 Withdrawn
486619360 Diameter: 7.75 Millimeter Withdrawn
486619395 Withdrawn
486619060 Diameter: 5.75 Millimeter 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