Advance®

ADVANCE® FIXATION PIN, HEADLES W/O GROOVE 80mm

Registry build 21.09.26
53manufacturers in China registered for this device type
64catalogue numbers in this listing
1recall

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 Advance®
Listed by Microport Orthopedics 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, Reprocessor, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Premarket notification Exempt
Record published 2016-10-28
Record revised 2019-11-05 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, manufacturing date

Catalogue Numbers

Catalogue numbers for Advance®
Catalogue number Size Status
K0001101 In distribution
K0060005 In distribution
K0040109 In distribution
K0017097 In distribution
K0002007 In distribution
K0027212 In distribution
K0027101 In distribution
K0000905 In distribution
OT001ADVC97 In distribution
KTIBSP63 In distribution
K0060002 In distribution
K0002000 In distribution
K0056011 In distribution
K0001012 In distribution
K0017065 In distribution
OT999ADVC97 In distribution
K0060003 In distribution
K0001010 In distribution
K0050033 In distribution
K0002006 In distribution
K0017210 In distribution
K0027213 In distribution
K0040117 In distribution
K0061082 In distribution
K0001009 In distribution
K0017200 In distribution
K0001003 In distribution
K0001288 In distribution
K0040114 In distribution
K0002011CN In distribution
K0063002 In distribution
K0017067 In distribution
K0012005 In distribution
K0017095 In distribution
K0040111 In distribution
K0061109 In distribution
K0056010 In distribution
K0031106 In distribution
K0015208 In distribution
K0002011 In distribution
K0060096 In distribution
K0060004 In distribution
K0000901 In distribution
K0017093 In distribution
K0002009 In distribution
K0060090 In distribution
K0060092 In distribution
K0001016 In distribution
K0050008 In distribution
K0040112 In distribution
K0001289 In distribution
K0040108 In distribution
K0060093 In distribution
K0021003 In distribution
K0017063 In distribution
K0001013 In distribution
K0017201 In distribution
K0002010 In distribution
K0060097 In distribution
K0001007 In distribution
K0021011 In distribution
K0056012 In distribution
K0031120 In distribution
K0002015 In distribution

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

1 of these is 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
2014-04-30 Class II Device Design Difficulty removing the cup adaptor from the impaction handle during surgery 140 units 2014-12-01

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