Stable-L™

Stable-L Torque Limiting AO Connect Handle

Registry build 21.09.26
14manufacturers in China registered for this device type
85catalogue numbers in this listing

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 Stable-L™
Listed by Nexus Spine, L.L.C., 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, Complaint-file establishment, Manufacturer
510(k) K212498
Record published 2022-04-30
Record revised 2025-02-24 (version 6)

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
Sizes Length 10 to 40 mm; width 4.9 to 41 mm; height 10 to 20 mm
Distribution end date 2025-02-21

Catalogue Numbers

Catalogue numbers for Stable-L™
Catalogue number Size Status
525098 Height 14 mm In distribution
525113 Height 12 mm In distribution
525076 Height 18 mm In distribution
525100 Height 18 mm In distribution
525096 Height 18 mm In distribution
525132 Width 4.9 mm In distribution
525099 Height 16 mm In distribution
525101 Height 20 mm In distribution
525134 Length 12 mm In distribution
525071 Height 18 mm In distribution
525106 Height 20 mm In distribution
525119 Height 16 mm In distribution
825074 In distribution
525082 Height 16 mm In distribution
525141 Width 4.9 mm In distribution
525097 Height 20 mm In distribution
525109 Height 14 mm In distribution
525137 Length 18 mm In distribution
525094 Height 14 mm In distribution
525131 Width 4.9 mm In distribution
525093 Height 12 mm In distribution
525117 Height 20 mm In distribution
525069 Height 14 mm In distribution
525116 Height 18 mm In distribution
525111 Height 18 mm In distribution
525077 Height 20 mm In distribution
525118 Height 14 mm In distribution
525127 Width 4.9 mm In distribution
525123 Height 18 mm In distribution
525140 Width 4.9 mm In distribution
825001 In distribution
525067 Height 10 mm In distribution
525091 Height 18 mm In distribution
525072 Height 20 mm In distribution
525135 Length 14 mm In distribution
525084 Height 20 mm In distribution
525121 Height 20 mm In distribution
525070 Height 16 mm In distribution
525114 Height 14 mm In distribution
525129 Width 4.9 mm In distribution
525105 Height 18 mm In distribution
525124 Height 20 mm In distribution
525130 Width 4.9 mm In distribution
525088 Height 12 mm In distribution
525138 Length 20 mm In distribution
525136 Length 16 mm In distribution
525120 Height 18 mm In distribution
525087 Height 10 mm In distribution
525083 Height 18 mm In distribution
525126 Height 20 mm In distribution
525074 Height 14 mm In distribution
525085 Height 18 mm In distribution
525075 Height 16 mm In distribution
525107 Height 10 mm In distribution
525090 Height 16 mm In distribution
525081 Height 20 mm In distribution
525089 Height 14 mm In distribution
525110 Height 16 mm In distribution
525103 Height 18 mm In distribution
525128 Width 4.9 mm In distribution
525108 Height 12 mm In distribution
525086 Height 20 mm In distribution
525092 Height 20 mm In distribution
525080 Height 18 mm In distribution
525115 Height 16 mm In distribution
525068 Height 12 mm In distribution
525102 Height 16 mm In distribution
525139 Width 4.9 mm In distribution
525104 Height 20 mm In distribution
525142 Width 4.9 mm In distribution
525079 Height 16 mm In distribution
525143 In distribution
525112 Height 20 mm In distribution
525133 Length 10 mm In distribution
525095 Height 16 mm In distribution
525125 Height 18 mm In distribution
525078 Height 14 mm In distribution
525122 Height 16 mm In distribution
525073 Height 12 mm In distribution
825115 Withdrawn
825095 Withdrawn
825100 Withdrawn
825000 Withdrawn
825098 Withdrawn
825117 Withdrawn

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

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