Aria

Specialty Reamer Distractor SET W/Thicker Cutting Edges

Registry build 21.09.26
53manufacturers in China registered for this device type
148catalogue 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 Aria
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 2019-11-27
Record revised 2026-03-19 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Prescription Prescription only
Label carries lot or batch number, manufacturing date
Sizes Length 40 to 160 mm; height 8 to 18 mm; width 12 to 22 mm; angle 0 to 8 °
Distribution end date 2025-10-13
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Aria
Catalogue number Size Status
48759040 In distribution
48755700 In distribution
48758530 In distribution
48759500 In distribution
48759050AA In distribution
IS4210ARI Length 40.0 mm In distribution
48759020AA In distribution
IS4039ARI Width 12.0 mm In distribution
IS4006ARI03 Length 160.0 mm In distribution
48759020 In distribution
IS4481REL In distribution
48759040AA In distribution
48755000 In distribution
48759020BB In distribution
IS2507ARI In distribution
48759600 In distribution
IS3079ARI03 Length 60.0 mm In distribution
IS4007ARI Length 160.0 mm In distribution
48759701 In distribution
48758540 In distribution
IS3151ARI In distribution
48759050 In distribution
IS3079ARI04 Height 16.0 mm In distribution
48755701 In distribution
IS3079ARI01 Length 60.0 mm In distribution
IS4006ARI01 Length 80.0 mm In distribution
IS4038ARI Height 18.0 mm In distribution
IS4422ARI Height 12.0 mm In distribution
48755005 In distribution
IS4042ARI Angle 8.0 ° In distribution
48759040BB In distribution
48759660 In distribution
48755400 In distribution
IS3079ARI02 Width 22.0 mm In distribution
IS3079ARI05 In distribution
48759360 In distribution
IS4006ARI02 Length 120.0 mm In distribution
48759030 In distribution
IS2508ARI In distribution
48755720 In distribution
48759912 Length 120.0 mm Withdrawn
48759927 Length 70.0 mm Withdrawn
48759928 Length 80.0 mm Withdrawn
48759410 Height 10.0 mm Withdrawn
48759359 Withdrawn
48758416 Height 16.0 mm Withdrawn
48759214 Height 14.0 mm Withdrawn
48759905 Length 50.0 mm Withdrawn
48758418 Length 50.0 mm Withdrawn
48759208 Height 8.0 mm Withdrawn
48755716 Length 160.0 mm Withdrawn
48758410 Length 50.0 mm Withdrawn
48755920 Length 120.0 mm Withdrawn
48759630 Withdrawn
48759916 Length 160.0 mm Withdrawn
48759614 Length 60.0 mm Withdrawn
48759935 Length 150.0 mm Withdrawn
48755100 Length 100.0 mm Withdrawn
48759934 Length 140.0 mm Withdrawn
48759308 Length 60.0 mm Withdrawn
48755870 Length 70.0 mm Withdrawn
48759616 Angle 0.0 ° Withdrawn
48759418 Width 22.0 mm Withdrawn
48755703 Withdrawn
48759906 Length 60.0 mm Withdrawn
48759108 Height 8.0 mm Withdrawn
48755060 Length 60.0 mm Withdrawn
48759408 Length 60.0 mm Withdrawn
48759210 Width 22.0 mm Withdrawn
48755930 Length 130.0 mm Withdrawn
48758218 Height 18.0 mm Withdrawn
48759926 Length 60.0 mm Withdrawn
48759909 Length 90.0 mm Withdrawn
48755950 Length 150.0 mm Withdrawn
48759110 Angle 0.0 ° Withdrawn
48755708 Length 80.0 mm Withdrawn
48758520 Withdrawn
48759508 Angle 0.0 ° Withdrawn
48758408 Height 8.0 mm Withdrawn
48758208 Length 60.0 mm Withdrawn
48758216 Height 16.0 mm Withdrawn
48755007 Withdrawn
48755130 Length 130.0 mm Withdrawn
48755140 Length 140.0 mm Withdrawn
48759218 Length 60.0 mm Withdrawn
48755850 Length 50.0 mm Withdrawn
48758412 Height 12.0 mm Withdrawn
48755960 Length 160.0 mm Withdrawn
48755890 Length 90.0 mm Withdrawn
48759610 Angle 0.0 ° Withdrawn
48759911 Length 110.0 mm Withdrawn
48759510 Width 18.0 mm Withdrawn
48755880 Length 80.0 mm Withdrawn
48755940 Length 140.0 mm Withdrawn
48759216 Angle 0.0 ° Withdrawn
48759618 Width 22.0 mm Withdrawn
48759925 Length 50.0 mm Withdrawn
48759414 Angle 8.0 ° Withdrawn
48755702 Withdrawn
48759416 Length 60.0 mm Withdrawn
48759608 Width 22.0 mm Withdrawn
48759318 Length 60.0 mm Withdrawn
48759908 Length 80.0 mm Withdrawn
48759316 Width 18.0 mm Withdrawn
48759312 Angle 8.0 ° Withdrawn
48759518 Length 60.0 mm Withdrawn
48755090 Length 90.0 mm Withdrawn
48759112 Angle 0.0 ° Withdrawn
48758414 Height 14.0 mm Withdrawn
48759212 Angle 0.0 ° Withdrawn
48755080 Length 80.0 mm Withdrawn
48759932 Length 120.0 mm Withdrawn
48759700 Withdrawn
48759930 Length 100.0 mm Withdrawn
48759314 Width 18.0 mm Withdrawn
48759514 Length 60.0 mm Withdrawn
48759310 Height 10.0 mm Withdrawn
48759612 Width 22.0 mm Withdrawn
48755150 Length 150.0 mm Withdrawn
48759116 Length 60.0 mm Withdrawn
48755070 Length 70.0 mm Withdrawn
48755710 Length 100.0 mm Withdrawn
48759516 Angle 0.0 ° Withdrawn
48755004 Withdrawn
48759915 Length 150.0 mm Withdrawn
48759412 Height 12.0 mm Withdrawn
48755160 Length 160.0 mm Withdrawn
48755050 Length 50.0 mm Withdrawn
48759118 Length 60.0 mm Withdrawn
48758212 Length 60.0 mm Withdrawn
48759933 Length 130.0 mm Withdrawn
48759114 Width 18.0 mm Withdrawn
48759913 Length 130.0 mm Withdrawn
48759907 Length 70.0 mm Withdrawn
48759931 Length 110.0 mm Withdrawn
48759914 Length 140.0 mm Withdrawn
48759512 Width 18.0 mm Withdrawn
48755860 Length 60.0 mm Withdrawn
48759929 Length 90.0 mm Withdrawn
48755900 Length 100.0 mm Withdrawn
48758214 Height 14.0 mm Withdrawn
48755712 Length 120.0 mm Withdrawn
48755910 Length 110.0 mm Withdrawn
48759936 Length 160.0 mm Withdrawn
48755110 Length 110.0 mm Withdrawn
48759910 Length 100.0 mm Withdrawn
48755120 Length 120.0 mm Withdrawn
48758210 Height 10.0 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