Vector™ Pedicle Screw System

Vector Instrument Set 1 - Al, SST, Nylon, Silicone, Radel

Registry build 21.09.26
15manufacturers in China registered for this device type
21catalogue numbers in this listing

Who Else Makes It

Concentrated in Jiangsu (6), Shanghai (3), Shandong (3). 6 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code NKB
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
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
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
Johnson & Johnson Medical (Depuy – Suzhou) Ltd. Suzhou Jiangsu Manufacturer 34
Shanghai Reach Medical Instrument Co., Ltd. Shanghai Shanghai Manufacturer 30
Changzhou Geasure Medical Apparatus AND Instruments Co., Ltd. Changzhou Jiangsu Contract manufacturer 25
Double Medical Technology Inc. Xiamen Fujian Contract manufacturer 14

Showing 12 of 15. All 15 manufacturers in China registered for Thoracolumbosacral Pedicle Screw System

Record

Regulatory record for Vector™ Pedicle Screw System
Listed by Inno-Health Technology Co., Ltd., Taiwan
FDA product code NKB
Device type Thoracolumbosacral Pedicle Screw System
Device class Class 2
Regulation 21 CFR 888.3070
Establishment Contract manufacturer, Contract steriliser, Manufacturer
510(k) K241276
Record published 2026-05-31

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, serial number
Sizes Outer diameter 5.5 mm; length 30 to 205 mm

Catalogue Numbers

Catalogue numbers for Vector™ Pedicle Screw System
Catalogue number Size Status
62-015535 Outer Diameter 5.5 mm In distribution
62-015545 Outer Diameter 5.5 mm In distribution
62-015550 Outer Diameter 5.5 mm In distribution
62-0155145 Outer Diameter 5.5 mm In distribution
62-0155135 Outer Diameter 5.5 mm In distribution
62-0155165 Outer Diameter 5.5 mm In distribution
BTA-202 In distribution
62-0155155 Outer Diameter 5.5 mm In distribution
62-0155205 Outer Diameter 5.5 mm In distribution
62-0155115 Outer Diameter 5.5 mm In distribution
62-0155120 Outer Diameter 5.5 mm In distribution
62-0155105 Outer Diameter 5.5 mm In distribution
62-0155110 Outer Diameter 5.5 mm In distribution
62-0155100 Outer Diameter 5.5 mm In distribution
62-0155125 Outer Diameter 5.5 mm In distribution
LS-749 In distribution
62-015530 Outer Diameter 5.5 mm In distribution
62-015540 Outer Diameter 5.5 mm In distribution
62-0155175 Outer Diameter 5.5 mm In distribution
62-0155195 Outer Diameter 5.5 mm In distribution
62-0155185 Outer Diameter 5.5 mm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
The Jasper Spinal Fixation System Gbs Commonwealth Co., Ltd. 32,491
Invictus Alphatec Spine, Inc. 4,722
Vital Spinal Fixation System Highridge Medical, LLC 4,422
Innoverse Spinal System CG MedTech Co., Ltd. 4,240
4CIS® Chiron Spinal Fixation System Alpha AI Co., Ltd. 3,787
LnK Spinal Fixation System L&K Biomed Co., Ltd. 3,522
Hedjet System Medyssey Co., Ltd. 3,438
Anax™ 5.5 Spinal System CG MedTech Co., Ltd. 3,424
Mega Plus MIS Spine System BK Meditech Co., Ltd. 3,396
ReLine Nuvasive, Inc. 2,882
Nex-D2 Next Orthosurgical 2,765
AnyPlus Spinal Fixation System GS Medical Co., Ltd. 2,386

Showing 12 of 1,490. All products under Thoracolumbosacral Pedicle Screw System

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of Vector™ Pedicle Screw System
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Innovasis, Inc. 510(k) number 2026-05-22 Class II Process design Pedicle screw system intended to provide immobilization/stabilization of spinal segments as adjunct to thoracic/lumbar/sacral spine fusion may have anti-torque instrument with undersized condition which could prevent mating tip from engagin 5

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