OrthoPediatrics Cannulated Screw System
Direct Measuring Device - 0.8 x 100mm/1.1 x 120mm Wires
Who Else Makes It
Concentrated in Jiangsu (15), Shanghai (5), Zhejiang (3). 19 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| MicroPort Orthopedics Global Supply Center Limited | Shanghai | Shanghai | Contract manufacturer | 82 |
| Apex (Guangzhou) Tools & Orthopedics Company | Guangzhou | Guangdong | Contract manufacturer | 62 |
| Changzhou Biomet Medical Devices Co., Ltd. | Changzhou | Jiangsu | Contract manufacturer | 54 |
| Canwell Medical Co., Ltd. | Jinhua | Zhejiang | Contract manufacturer | 42 |
| Suzhou Elite Precision Machinery Co., Ltd. | Kunshan | Jiangsu | Contract manufacturer | 35 |
| B-ONE Medical (Suzhou) Co., Ltd. | Suzhou | Jiangsu | Contract manufacturer | 23 |
| LX Precision Shanghai Co Ltd | Shanghai | Shanghai | Contract manufacturer | 19 |
| Stryker (Suzhou) Medical Technology Co., Ltd. | Suzhou | Jiangsu | Contract manufacturer | 19 |
| Suzhou Ahno Medical Devices Co., Ltd. | Suzhou | Jiangsu | Contract manufacturer | 17 |
| Zibo Dante Co., Ltd. | Zibo | Shandong | Contract manufacturer | 17 |
| Sanbor Medical Xiamen, Inc. | Xiamen | Fujian | Contract manufacturer | 16 |
| Suzhou Kangli Orthopaedics Instrument Co., Ltd. | Zhangjiagang | Jiangsu | Contract manufacturer | 11 |
Showing 12 of 31. All 31 manufacturers in China registered for Screw, Fixation, Bone
Record
| Listed by | Orthopediatrics, Corp, United States |
|---|---|
| FDA product code | HWC |
| Device type | Screw, Fixation, Bone |
| Device class | Class 2 |
| Regulation | 21 CFR 888.3040 |
| Establishment | Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer |
| 510(k) | K190324 |
| Record published | 2019-09-03 |
| Record revised | 2024-11-26 (version 4) |
Specifications
| MRI safety | MR Conditional |
|---|---|
| Sterilisation | Moist Heat or Steam Sterilization |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number |
| UDI direct marking | Exempt |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 00-1400-2614 | In distribution | |
| 00-1400-2524 | In distribution | |
| 00-1400-4562 | In distribution | |
| 00-1400-6720 | In distribution | |
| 00-1400-5890 | In distribution | |
| 00-1402-6146 | In distribution | |
| 00-1402-5084 | In distribution | |
| 01-1400-0020 | In distribution | |
| 00-1402-6044 | In distribution | |
| 00-1402-1075 | In distribution | |
| 00-1400-5700 | In distribution | |
| 00-1400-3632 | In distribution | |
| 01-1400-1030 | In distribution | |
| 00-1402-2030 | In distribution | |
| 00-1400-3552 | In distribution | |
| 00-1402-6126 | In distribution | |
| 00-1400-3550 | In distribution | |
| 00-1400-4042 | In distribution | |
| 01-1400-0115 | In distribution | |
| 00-1400-4126 | In distribution | |
| 00-1400-4124 | In distribution | |
| 00-1400-5906 | In distribution | |
| 00-1402-5122 | In distribution | |
| 00-1400-3236 | In distribution | |
| 00-1400-3240 | In distribution | |
| 00-1400-5442 | In distribution | |
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| 00-1400-4148 | In distribution | |
| 00-1402-2140 | In distribution | |
| 01-1400-0039 | In distribution | |
| 00-1400-6835 | In distribution | |
| 00-1400-5854 | In distribution | |
| 00-1400-4772 | In distribution | |
| 00-1400-6562 | In distribution | |
| 00-1400-4552 | In distribution | |
| 00-1402-1090 | In distribution | |
| 00-1400-2712 | In distribution | |
| 00-1400-3132 | In distribution | |
| 00-1402-5134 | In distribution | |
| 00-1400-5914 | In distribution | |
| 00-1400-5834 | In distribution | |
| 01-1400-0130 | In distribution | |
| 00-1400-3126 | In distribution | |
| 00-1400-6666 | In distribution | |
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| 00-1400-4038 | In distribution | |
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Showing 250 of 300 catalogue numbers.
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Screw, Fixation, Bone | Synthes Gmbh | 3,975 |
| Aptus | Medartis Inc. | 3,623 |
| Acumed | Acumed LLC | 3,187 |
| Arthrex® | Arthrex, Inc. | 2,781 |
| OsteoMed | Osteomed | 2,764 |
| Screw, Fixation, Bone | AAP Implantate AG | 2,176 |
| Screw, Fixation, Bone | Zimmer, Inc. | 1,993 |
| Arix System Bone Screw | Jeil Medical Corporation | 1,875 |
| Cannulated Screw System + | Tyber Medical | 1,814 |
| Cannulated Compression Headless Screw | Tyber Medical | 1,621 |
| Microware Bone Plates and Bone Screws | Microware Precision Co., Ltd. | 1,601 |
| Anthem | Globus Medical, Inc. | 1,538 |
Showing 12 of 5,775. All products under Screw, Fixation, Bone
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K190324 | 2019-07-05 |
| K082949 | 2008-11-25 |
Recalls
7 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.
| Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|
| 2016-07-27 | Class II | Labeling mix-ups | OrthoPediatrics Corp.is voluntarily recalling multiple lots of the 3.5mm Bowed Locking Compression Femur 14-hole Plate and 18-hole Plate due to the devices being mislabeled. | 41 | 2017-03-24 |
| 2016-07-27 | Class II | Labeling mix-ups | OrthoPediatrics Corp.is voluntarily recalling multiple lots of the 3.5mm Bowed Locking Compression Femur 14-hole Plate and 18-hole Plate due to the devices being mislabeled. | 41 | 2017-03-24 |
| 2014-01-08 | Class II | Labeling mix-ups | OrthoPediatrics has initiated a Voluntary RECALL of Part # 00-0903-2620, 3.5MM Locking Cortical Screw, Lot # 009SV because the device within the package may be incorrect. These packages incorrectly contain a 3.5mm Non Locking Cortical Scre | 12 units | 2014-04-23 |
| 2013-07-24 | Class II | Process design | OrthoPediatrics has initiated a voluntary recall of Part # 01-1050-002, 2.5mm Drill Bit, Lot #91300335. Only drill bits that are in their original packaging are being recalled. The description on the package of this drill bit has a wrong si | 68 | 2013-08-26 |
| 2013-04-19 | Class II | Device Design | Post Market Surveillance of the 90 degree Cannulated Infant Blade Plate indicated that there have been five reports concerning bending of the plate intra-operatively. | 130 devices were shipped | 2013-09-19 |
| 2013-04-19 | Class II | Device Design | Post Market Surveillance of the 90 degree Cannulated Infant Blade Plate indicated that there have been five reports concerning bending of the plate intra-operatively. | 130 devices were shipped | 2013-09-19 |
| 2013-04-19 | Class II | Device Design | Post Market Surveillance of the 90 degree Cannulated Infant Blade Plate indicated that there have been five reports concerning bending of the plate intra-operatively. | 130 devices were shipped | 2013-09-19 |
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.