Newport

Cannulated Reduction Polyaxial Screw, Ø6.5 x 105mm

Registry build 21.09.26
13manufacturers in China registered for this device type
62catalogue numbers in this listing
3510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (7), Shanghai (2), Shandong (2). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code MNI
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
APS Materials Suzhou Suzhou Jiangsu Contract manufacturer 18
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Johnson & Johnson Medical (Depuy – Suzhou) Ltd. Suzhou Jiangsu Manufacturer 34
Double Medical Technology Inc. Xiamen Fujian Contract manufacturer 14
Suzhou Kangli Orthopaedics Instrument Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 11
Changzhou Yonghua Medical Instruments Co., Ltd. Changzhou Jiangsu Manufacturer 8
Jiangsu Ideal Medical Science & Technology Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 7

Showing 12 of 13. All 13 manufacturers in China registered for Orthosis, Spinal Pedicle Fixation

Record

Regulatory record for Newport
Listed by Seaspine, Inc., United States
FDA product code MNI
Device type Orthosis, Spinal Pedicle Fixation
Device class Class 2
Regulation 21 CFR 888.3070
Record published 2017-02-13
Record revised 2025-07-02 (version 3)

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
Distribution end date 2017-02-13

Catalogue Numbers

Catalogue numbers for Newport
Catalogue number Size Status
63-6030 Ø6.0 x 30mm Withdrawn
63-7040 Ø7.0 x 40mm Withdrawn
62-7070 Ø7.0 x 70mm Withdrawn
63-6530 Ø6.5 x 30mm Withdrawn
63-7595 Ø7.5 x 95mm Withdrawn
62-6505 Ø6.5 x 105mm Withdrawn
63-6550 Ø6.5 x 50mm Withdrawn
63-6540 Ø6.5 x 40mm Withdrawn
63-6595 Ø6.5 x 95mm Withdrawn
62-7595 Ø7.5 x 95mm Withdrawn
63-7535 Ø7.5 x 35mm Withdrawn
62-7565 Ø7.5 x 65mm Withdrawn
63-7545 Ø7.5 x 45mm Withdrawn
62-5530 Ø5.5 x 30mm Withdrawn
62-7050 Ø7.0 x 50mm Withdrawn
62-6585 Ø6.5 x 85mm Withdrawn
62-7040 Ø7.0 x 40mm Withdrawn
62-7545 Ø7.5 x 45mm Withdrawn
63-7070 Ø7.0 x 70mm Withdrawn
62-5550 Ø5.5 x 50mm Withdrawn
63-6570 Ø6.5 x 70mm Withdrawn
63-7050 Ø7.0 x 50mm Withdrawn
62-5540 Ø5.5 x 40mm Withdrawn
62-7030 Ø7.0 x 30mm Withdrawn
62-6555 Ø6.5 x 55mm Withdrawn
63-7505 Ø7.5 x 105mm Withdrawn
63-7060 Ø7.0 x 60mm Withdrawn
63-5530 Ø5.5 x 30mm Withdrawn
62-6545 Ø6.5 x 45mm Withdrawn
62-5560 Ø5.5 x 60mm Withdrawn
63-7575 Ø7.5 x 75mm Withdrawn
61-7595 DIA 7.5 x 95mm Withdrawn
63-6040 Ø6.0 x 40mm Withdrawn
62-7535 Ø7.5 x 35mm Withdrawn
62-7555 Ø7.5 x 55mm Withdrawn
63-7555 Ø7.5 x 55mm Withdrawn
62-6050 Ø6.0 x 50mm Withdrawn
63-6505 Ø6.5 x 105mm Withdrawn
63-6580 Ø6.5 x 80mm Withdrawn
62-6575 Ø6.5 x 75mm Withdrawn
63-6050 Ø6.0 x 50mm Withdrawn
63-7030 Ø7.0 x 30mm Withdrawn
63-6560 Ø6.5 x 60mm Withdrawn
62-6030 Ø6.0 x 30mm Withdrawn
63-6060 Ø6.0 x 60mm Withdrawn
62-7575 Ø7.5 x 75mm Withdrawn
62-6525 Ø6.5 x 25mm Withdrawn
63-7565 Ø7.5 x 65mm Withdrawn
62-7585 Ø7.5 x 85mm Withdrawn
63-5550 Ø5.5 x 50mm Withdrawn
63-5560 Ø5.5 x 60mm Withdrawn
62-6595 Ø6.5 x 95mm Withdrawn
63-7525 Ø7.5 x 25mm Withdrawn
63-7585 Ø7.5 x 85mm Withdrawn
62-7060 Ø7.0 x 60mm Withdrawn
62-6060 Ø6.0 x 60mm Withdrawn
62-6565 Ø6.5 x 65mm Withdrawn
63-5540 Ø5.5 x 40mm Withdrawn
62-7525 Ø7.5 x 25mm Withdrawn
62-6040 Ø6.0 x 40mm Withdrawn
62-7505 Ø7.5 x 105mm Withdrawn
62-6535 Ø6.5 x 35mm Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
CD Horizon® Spinal System Medtronic Sofamor Danek, Inc. 2,342
Creo Globus Medical, Inc. 1,784
ReLine Nuvasive, Inc. 1,718
AnyPlus Spinal Fixation System GS Medical Co., Ltd. 1,525
Apex Spine System Spinecraft LLC 1,114
Revere Globus Medical, Inc. 1,051
LnK Spinal Fixation System L&K Biomed Co., Ltd. 974
LnK Basic Spinal Fixation System L&K Biomed Co., Ltd. 935
Arsenal Alphatec Spine, Inc. 932
Zavation Zavation 864
Polaris™ 5.5 Spinal System Biomet Spine 809
Apex-DL Spine System Spinecraft LLC 792

Showing 12 of 950. All products under Orthosis, Spinal Pedicle Fixation

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K062934 2006-11-16
K032739 2003-11-20
K031381 2003-07-30

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