Idys™- Plif

72 catalogue numbers from 04714213, listed by Clariance, Inc., United States, under Intervertebral Fusion Device With Bone Graft, Lumbar. 14 manufacturers in China are registered for this product code.

Registry build 21.09.26
14manufacturers in China registered for this device type
72catalogue numbers in this listing
6510(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 Idys™- Plif
Listed by Clariance, Inc., 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 Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K243670
Record published 2018-05-21

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, manufacturing date
Sizes Height 5 to 16 mm; length 6 to 25 mm; outer diameter 6 to 16 mm

Catalogue Numbers

Catalogue numbers for Idys™- Plif
Catalogue number Size Status
04714213 Height 13 mm In distribution
04707016 Height 16 mm In distribution
04522008 In distribution
04707007 Height 7 mm In distribution
04714208 Length 20 mm In distribution
04705010 Length 10 mm In distribution
04709008 Height 8 mm In distribution
04704015 Height 5 mm In distribution
04762000 In distribution
04707116 Outer Diameter 16 mm In distribution
04522012 In distribution
04522513 In distribution
04715002 In distribution
04522509 In distribution
04714313 Height 13 mm In distribution
04714310 Length 25 mm In distribution
04709012 Height 12 mm In distribution
04709015 Height 15 mm In distribution
04522511 In distribution
04709007 Height 7 mm In distribution
04714209 Height 9 mm In distribution
04714311 Height 11 mm In distribution
04709016 Height 16 mm In distribution
04522013 In distribution
04715003 In distribution
04707110 Outer Diameter 10 mm In distribution
04707108 Outer Diameter 8 mm In distribution
04781008 Length 8 mm In distribution
04522010 In distribution
04714210 Length 20 mm In distribution
04709014 Height 14 mm In distribution
04709011 Height 11 mm In distribution
04707011 Height 11 mm In distribution
04709009 Height 9 mm In distribution
04714312 Length 25 mm In distribution
04704005 Height 5 mm In distribution
04707113 Outer Diameter 13 mm In distribution
04522009 In distribution
04761000 Length 20 mm In distribution
04707112 Outer Diameter 12 mm In distribution
04522514 In distribution
04714212 Length 20 mm In distribution
04522011 In distribution
04714211 Height 11 mm In distribution
04707109 Outer Diameter 9 mm In distribution
04714314 Length 25 mm In distribution
04707010 Height 10 mm In distribution
04522508 In distribution
04761001 Length 25 mm In distribution
04707008 Height 8 mm In distribution
04707111 Outer Diameter 11 mm In distribution
04716001 In distribution
04705011 In distribution
04522510 In distribution
04709013 Height 13 mm In distribution
04717003 Length 20 mm In distribution
04714308 Length 25 mm In distribution
04709010 Height 10 mm In distribution
04522512 In distribution
04707107 Outer Diameter 7 mm In distribution
04709006 Height 6 mm In distribution
04707009 Height 9 mm In distribution
04707006 Height 6 mm In distribution
04714309 Height 9 mm In distribution
04781006 Length 6 mm In distribution
04707013 Height 13 mm In distribution
04707012 Height 12 mm In distribution
04707015 Height 15 mm In distribution
04707106 Outer Diameter 6 mm In distribution
04707014 Height 14 mm In distribution
04707115 Outer Diameter 15 mm In distribution
04707114 Outer Diameter 14 mm 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
K243670 2024-12-31
K200919 2021-04-12
K200920 2020-05-29
K183259 2019-03-01
K172465 2017-12-15
K131178 2013-10-10

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