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