Valeo II PL OL Interbody Fusion System

Valeo II PL OL Positioner Tip (PEEK)

Registry build 21.09.26
14manufacturers in China registered for this device type
198catalogue numbers in this listing
4510(k) clearances naming this product code
4recalls on this code

Who Else Makes It

Concentrated in Jiangsu (6), Shandong (2), Shanghai (2). 7 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code MAX
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Suzhou Ahno Medical Devices Co., Ltd. Suzhou Jiangsu Contract manufacturer 17
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Jiangsu Ideal Medical Science & Technology Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 7
Zhisu Health Tech Jiaxing Co., Ltd. Tongxiang Zhejiang Contract manufacturer 4
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
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
Zhejiang Decans Medical Devices Co., Ltd. Jiaxing Zhejiang Manufacturer 10

Showing 12 of 14. All 14 manufacturers in China registered for Intervertebral Fusion Device With Bone Graft, Lumbar

Record

Regulatory record for Valeo II PL OL Interbody Fusion System
Listed by CTL Medical Corporation, United States
FDA product code MAX
Device type Intervertebral Fusion Device With Bone Graft, Lumbar
Device class Class 2
Regulation 21 CFR 888.3080
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K082801
Record published 2023-09-27
Record revised 2026-04-24 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Label carries lot or batch number, expiry date, manufacturing date

Catalogue Numbers

Catalogue numbers for Valeo II PL OL Interbody Fusion System
Catalogue number Size Status
12.301.2508 In distribution
12.302.1511 In distribution
12.302.0511 In distribution
11.113.4814 In distribution
11.113.2517 In distribution
11.113.5008 In distribution
11.113.5010 In distribution
12.301.2513 In distribution
12.301.2510 In distribution
11.113.5014 In distribution
11.113.3808 In distribution
037.7032 In distribution
12.300.1011 In distribution
11.113.2519 In distribution
12.301.1013 In distribution
12.300.1508 In distribution
12.302.1509 In distribution
12.300.2515 In distribution
11.113.3813 In distribution
11.113.2507 In distribution
12.302.2511 In distribution
11.113.5015 In distribution
11.113.2511 In distribution
11.113.2518 In distribution
037.7033 In distribution
12.301.2008 In distribution
12.301.1508 In distribution
12.300.2509 In distribution
12.301.1509 In distribution
91.000.9009 In distribution
12.302.0516 In distribution
12.301.1515 In distribution
12.301.1511 In distribution
12.302.1513 In distribution
11.113.1814 In distribution
12.301.2016 In distribution
12.301.2515 In distribution
12.302.1516 In distribution
12.302.0512 In distribution
11.113.1810 In distribution
037.7029 In distribution
11.113.6008 In distribution
11.113.4815 In distribution
11.113.6013 In distribution
11.113.5011 In distribution
12.301.1510 In distribution
12.302.0508 In distribution
12.301.1512 In distribution
037.7030 In distribution
12.301.1009 In distribution
11.113.5013 In distribution
11.113.1808 In distribution
12.302.2515 In distribution
11.113.6012 In distribution
11.113.4509 In distribution
12.300.2007 In distribution
12.302.1514 In distribution
037.7071 In distribution
11.113.3814 In distribution
11.113.4613 In distribution
037.7073 In distribution
037.7072 In distribution
11.113.4513 In distribution
11.113.3815 In distribution
12.301.2516 In distribution
12.300.2015 In distribution
12.300.1014 In distribution
12.302.0509 In distribution
11.113.5007 In distribution
11.113.3811 In distribution
12.301.2011 In distribution
11.113.1813 In distribution
11.113.5009 In distribution
12.301.2010 In distribution
11.113.1807 In distribution
037.7074 In distribution
12.300.1511 In distribution
12.300.2512 In distribution
91.113.6022 In distribution
12.300.1013 In distribution
12.300.2009 In distribution
12.301.1513 In distribution
11.113.4514 In distribution
11.113.4515 In distribution
11.113.3810 In distribution
11.113.6010 In distribution
12.300.2012 In distribution
12.300.2010 In distribution
037.7034 In distribution
11.113.6011 In distribution
12.300.1509 In distribution
12.300.1515 In distribution
12.301.2007 In distribution
12.301.2009 In distribution
12.301.2014 In distribution
12.302.1512 In distribution
12.300.2016 In distribution
037.7056 In distribution
11.113.4714 In distribution
11.113.6015 In distribution
12.302.0514 In distribution
037.7052 In distribution
037.7053 In distribution
12.300.1008 In distribution
12.302.0513 In distribution
037.7076 In distribution
11.113.3807 In distribution
11.113.4511 In distribution
12.301.1012 In distribution
12.302.1510 In distribution
037.7031 In distribution
12.300.1516 In distribution
12.300.2014 In distribution
11.113.1811 In distribution
12.300.1012 In distribution
12.300.1512 In distribution
037.7070 In distribution
12.301.2509 In distribution
12.300.1009 In distribution
11.113.1812 In distribution
037.7028 In distribution
12.301.1514 In distribution
12.301.1011 In distribution
12.302.2513 In distribution
12.301.1014 In distribution
12.300.1513 In distribution
12.300.1007 In distribution
12.300.1010 In distribution
11.113.4510 In distribution
12.300.2510 In distribution
12.302.1515 In distribution
11.113.2515 In distribution
12.300.2008 In distribution
12.302.2514 In distribution
12.301.1008 In distribution
11.113.5012 In distribution
12.302.0510 In distribution
12.300.1015 In distribution
037.7069 In distribution
12.300.2508 In distribution
12.301.2012 In distribution
12.301.2512 In distribution
11.113.6009 In distribution
12.302.0515 In distribution
037.7035 In distribution
11.113.2509 In distribution
11.113.2510 In distribution
037.7025 In distribution
12.301.2015 In distribution
12.302.2508 In distribution
12.302.1508 In distribution
12.302.2516 In distribution
12.301.2514 In distribution
037.7054 In distribution
037.7075 In distribution
037.7050 In distribution
12.302.2512 In distribution
12.300.2013 In distribution
11.113.6007 In distribution
91.113.6005 In distribution
11.113.3809 In distribution
11.113.4812 In distribution
12.300.1510 In distribution
037.7036 In distribution
11.113.6014 In distribution
037.7055 In distribution
12.301.1516 In distribution
037.7049 In distribution
11.113.2512 In distribution
12.300.1514 In distribution
037.7294 In distribution
12.302.2509 In distribution
12.301.1015 In distribution
12.300.1016 In distribution
11.113.4715 In distribution
11.113.2508 In distribution
12.301.1010 In distribution
11.113.1815 In distribution
12.300.2516 In distribution
11.113.4712 In distribution
12.300.2514 In distribution
11.113.1809 In distribution
12.300.2513 In distribution
11.113.4512 In distribution
12.300.2011 In distribution
12.301.1016 In distribution
11.113.2516 In distribution
12.301.2013 In distribution
11.113.2513 In distribution
12.301.2511 In distribution
11.113.2520 In distribution
11.113.4508 In distribution
11.113.3812 In distribution
12.300.2511 In distribution
11.113.2514 In distribution
037.7051 In distribution
12.301.1007 In distribution
12.302.2510 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Peridot Intervertebral body fusion system Gbs Commonwealth Co., Ltd. 10,850
Yellowstone Summit Spine 6,654
CoRoent Nuvasive, Inc. 5,690
Zavation Zavation 2,554
Anyplus II Spinal Fixation System GS Medical Co., Ltd. 2,533
Talos® IBF Meditech Spine, LLC 2,163
Peridot-PT Intervertebral body fusion system Gbs Commonwealth Co., Ltd. 1,956
TirboLOX-L Lumbar Ibfd Captiva Spine, Inc. 1,926
Endoskeleton® TL Titan Spine, LLC 1,896
Evos Lumbar Interbody System Cutting Edge Spine 1,871
Epiphany Pantheon Spinal LLC 1,507
LnK Lumbar Interbody Fusion Cage System L&K Biomed Co., Ltd. 1,506

Showing 12 of 1,958. All products under Intervertebral Fusion Device With Bone Graft, Lumbar

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K233947 2024-10-10
K231359 2023-06-09
K213641 2022-09-15
K192863 2020-08-26

Recalls

4 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.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity
2019-08-21 Class II Device Design Reports received of the device fracturing during insertion. 46 units
2019-08-21 Class II Device Design Reports received of the device fracturing during insertion. 45 units
2019-08-21 Class II Device Design Reports received of the device fracturing during insertion. 39 units
2019-08-21 Class II Device Design Reports received of the device fracturing during insertion. 39 units

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P000028 2004-06-18 AFFINITY ANTERIOR CERVICAL CAGE SYSTEM Medtronic Sofamor Danek USA, Inc.
P970015 2003-09-10 LT-CAGE PEEK LUMBAR TAPERED FUSION DEVICE Sofamor Danek
P980048 2001-04-20 BAK/CERVICAL (BAK/C) INTERBODY FUSION SYSTEM Sulzer Spine-Tech
P950019 1999-03-19 RAY THREADED FUSION CAGE (TFC) DEVICE WITH INSTRUMENTATION Stryker Spine
P950002 1997-06-30 BAK INTERBODY FUSION SYSTEM Zimmer Spine, Inc.

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