Slpss

SLPSS Non-Cannulated Instrument and Implant Set

Registry build 21.09.26
15manufacturers in China registered for this device type
52catalogue numbers in this listing
11510(k) clearances naming this product code
22recalls on this code

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 Slpss
Listed by Spinal Elements, Inc., United States
FDA product code NKB
Device type Thoracolumbosacral Pedicle Screw System
Device class Class 2
Regulation 21 CFR 888.3070
Establishment Specification developer, Complaint-file establishment, Manufacturer
Record published 2017-08-10
Record revised 2025-07-02 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Label carries lot or batch number

Catalogue Numbers

Catalogue numbers for Slpss
Catalogue number Size Status
8235-45-C In distribution
8235-125-S In distribution
8196-6565C In distribution
8196-7550C In distribution
8196-7065 In distribution
8196-7050 In distribution
8196-7055 In distribution
8235-200-S In distribution
SLPSS-NC In distribution
SLPSS-C In distribution
8196-7560C In distribution
8196-7555 In distribution
8235-85-C In distribution
8196-6560 In distribution
8196-7560 In distribution
8235-150-S In distribution
8196-7545C In distribution
8196-6540C In distribution
8196-6550 In distribution
8196-7045 In distribution
8235-45-S In distribution
8196-6550C In distribution
8196-7555C In distribution
8196-7540C In distribution
8235-55-C In distribution
8196-6560C In distribution
8196-6545 In distribution
8235-75-C In distribution
8196-6555C In distribution
8196-5550 In distribution
8235-85-S In distribution
8235-100-S In distribution
8235-35-S In distribution
8196-6565 In distribution
8196-6555 In distribution
8196-7565C In distribution
8196-7565 In distribution
8219-1 In distribution
8196-7540 In distribution
8196-6545C In distribution
8196-5540 In distribution
8196-7545 In distribution
8235-55-S In distribution
8219 In distribution
8196-7550 In distribution
8196-5545 In distribution
8235-65-S In distribution
8235-65-C In distribution
8196-7040 In distribution
8235-75-S In distribution
8196-6540 In distribution
8196-7060 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

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K243916 2025-02-21
K222516 2022-12-01
K191576 2019-09-16
K172967 2018-04-10
K151215 2015-06-03
K141372 2014-08-22
K120467 2012-07-30
K091587 2009-07-01
K082353 2009-01-22
K083230 2008-12-03
K071914 2007-10-12

Recalls

22 of these are Class III. Class III is unlikely to cause harm at all → typically a labelling or documentation fault. 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
2015-04-09 Class III Under Investigation by firm Some rods may not meet the appropriate traceability requirements including the lot number. Some rods were found to not include the product identification number (product number and lot number) marked directly on the rod. The lack of marki 588 2015-06-25
2009-04-17 Class III Nonconforming Material/Component Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue. 68 units total 2013-05-07
2009-04-17 Class III Nonconforming Material/Component Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue. 68 units total 2013-05-07
2009-04-17 Class III Nonconforming Material/Component Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue. 68 units total 2013-05-07
2009-04-17 Class III Nonconforming Material/Component Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue. 68 units total 2013-05-07
2009-04-17 Class III Nonconforming Material/Component Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue. 68 units total 2013-05-07
2009-04-17 Class III Nonconforming Material/Component Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue. 68 units total 2013-05-07
2009-04-17 Class III Nonconforming Material/Component Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue. 68 units total 2013-05-07
2009-04-17 Class III Nonconforming Material/Component Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue. 68 units total 2013-05-07
2009-04-17 Class III Nonconforming Material/Component Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue. 68 units total 2013-05-07
2009-04-17 Class III Nonconforming Material/Component Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue. 68 units total 2013-05-07
2009-04-17 Class III Nonconforming Material/Component Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue. 68 units total 2013-05-07
2009-04-17 Class III Nonconforming Material/Component Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue. 68 units total 2013-05-07
2009-04-17 Class III Nonconforming Material/Component Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue. 68 units total 2013-05-07
2009-04-17 Class III Nonconforming Material/Component Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue. 68 units total 2013-05-07
2009-04-17 Class III Nonconforming Material/Component Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue. 68 units total 2013-05-07
2009-04-17 Class III Nonconforming Material/Component Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue. 68 units total 2013-05-07
2009-04-17 Class III Nonconforming Material/Component Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue. 68 units total 2013-05-07
2009-04-17 Class III Nonconforming Material/Component Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue. 68 units total 2013-05-07
2009-04-17 Class III Nonconforming Material/Component Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue. 68 units total 2013-05-07
2009-04-17 Class III Nonconforming Material/Component Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue. 68 units total 2013-05-07
2009-04-17 Class III Nonconforming Material/Component Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue. 68 units total 2013-05-07

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