MectaLIF 3d

MectaLIF Posterior 3D 11x25x14 L10°

Registry build 21.09.26
14manufacturers in China registered for this device type
613catalogue numbers in this listing
3510(k) clearances naming this product 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 MectaLIF 3D
Listed by Medacta International SA, Switzerland
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, Private-label distributor, Complaint-file establishment, Manufacturer, Exporter
510(k) K251016
Record published 2025-07-25

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date

Catalogue Numbers

Catalogue numbers for MectaLIF 3D
Catalogue number Size Status
03.44.006 In distribution
03.43.025 In distribution
03.43.068 In distribution
03.43.072 In distribution
03.41.311 In distribution
03.41.006 In distribution
03.41.113 In distribution
03.41.276 In distribution
03.41.038 In distribution
03.44.001 In distribution
03.41.053 In distribution
03.43.128 In distribution
03.43.202 In distribution
03.43.265 In distribution
03.43.235 In distribution
03.43.324 In distribution
03.41.022 In distribution
03.43.295 In distribution
03.43.261 In distribution
03.44.031 In distribution
03.41.231 In distribution
03.41.030 In distribution
03.41.244 In distribution
03.43.231 In distribution
03.41.080 In distribution
03.41.064 In distribution
03.41.227 In distribution
03.41.316 In distribution
03.43.332 In distribution
03.41.114 In distribution
03.43.318 In distribution
03.41.085 In distribution
03.43.233 In distribution
03.41.078 In distribution
03.41.101 In distribution
03.41.105 In distribution
03.43.312 In distribution
03.43.287 In distribution
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03.43.250 In distribution
03.41.106 In distribution
03.43.045 In distribution
03.43.352 In distribution
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03.43.254 In distribution
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03.43.059 In distribution
03.41.028 In distribution
03.41.117 In distribution
03.44.022 In distribution
03.43.105 In distribution
03.41.273 In distribution
03.44.044 In distribution
03.43.158 In distribution
03.44.020 In distribution
03.41.044 In distribution
03.41.205 In distribution
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03.41.016 In distribution
03.43.225 In distribution
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03.43.028 In distribution
03.43.113 In distribution
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03.41.255 In distribution
03.41.035 In distribution
03.41.228 In distribution
03.43.291 In distribution
03.43.055 In distribution
03.43.272 In distribution
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03.41.120 In distribution
03.43.018 In distribution
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03.43.322 In distribution
03.43.310 In distribution
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03.43.008 In distribution
03.44.004 In distribution
03.41.055 In distribution
03.41.054 In distribution
03.43.090 In distribution
03.41.216 In distribution
03.41.305 In distribution
03.41.230 In distribution
03.41.119 In distribution
03.43.031 In distribution
03.43.034 In distribution
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03.43.006 In distribution
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03.41.099 In distribution
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03.41.103 In distribution
03.41.033 In distribution
03.43.245 In distribution
03.43.154 In distribution
03.41.275 In distribution
03.43.124 In distribution
03.41.123 In distribution
03.43.311 In distribution
03.41.029 In distribution
03.43.046 In distribution
03.43.094 In distribution
03.43.204 In distribution
03.43.056 In distribution
03.43.347 In distribution
03.43.135 In distribution
03.43.042 In distribution
03.44.018 In distribution
03.43.131 In distribution
03.41.238 In distribution
03.43.277 In distribution
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03.41.264 In distribution
03.43.320 In distribution
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03.41.259 In distribution
03.43.074 In distribution
03.44.029 In distribution
03.41.025 In distribution
03.44.003 In distribution
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03.41.250 In distribution
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03.43.206 In distribution
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03.41.300 In distribution
03.41.003 In distribution
03.41.018 In distribution
03.41.295 In distribution
03.43.313 In distribution
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03.41.020 In distribution
03.43.013 In distribution
03.43.099 In distribution
03.41.265 In distribution
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03.43.300 In distribution
03.43.092 In distribution
03.41.315 In distribution
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03.44.015 In distribution
03.44.036 In distribution
03.43.100 In distribution
03.43.134 In distribution
03.43.253 In distribution
03.44.034 In distribution
03.41.060 In distribution
03.41.268 In distribution
03.41.218 In distribution
03.41.222 In distribution
03.41.011 In distribution
03.41.100 In distribution
03.41.066 In distribution
03.43.326 In distribution
03.43.351 In distribution
03.43.363 In distribution
03.41.320 In distribution
03.41.031 In distribution
03.41.263 In distribution
03.43.052 In distribution
03.43.047 In distribution
03.43.010 In distribution
03.43.278 In distribution
03.43.060 In distribution
03.44.030 In distribution
03.41.075 In distribution
03.41.253 In distribution
03.43.146 In distribution
03.43.050 In distribution
03.43.017 In distribution
03.41.261 In distribution
03.43.089 In distribution
03.41.260 In distribution
03.43.125 In distribution
03.43.054 In distribution
03.43.275 In distribution
03.41.125 In distribution
03.44.043 In distribution
03.43.078 In distribution
03.43.205 In distribution
03.43.096 In distribution
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03.41.262 In distribution
03.41.122 In distribution
03.43.049 In distribution
03.43.337 In distribution
03.41.056 In distribution
03.41.088 In distribution
03.41.046 In distribution
03.43.276 In distribution
03.43.333 In distribution
03.43.286 In distribution
03.44.017 In distribution
03.43.041 In distribution
03.43.086 In distribution
03.41.308 In distribution
03.43.005 In distribution
03.41.116 In distribution
03.43.084 In distribution
03.43.244 In distribution

Showing 250 of 300 catalogue numbers.

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
K133192 2014-01-30
K131671 2013-07-05
K110927 2011-06-13

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