EIT Llif Trial

Trial, H 12mm, 16°, 45/22

Registry build 21.09.26
14manufacturers in China registered for this device type
121catalogue numbers in this listing
5510(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 EIT Llif Trial
Listed by EIT Emerging Implant Technologies Gmbh, Germany
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, Manufacturer
Record published 2018-11-28
Record revised 2019-02-07 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Prescription Prescription only
Label carries lot or batch number, manufacturing date

Catalogue Numbers

Catalogue numbers for EIT Llif Trial
Catalogue number Size Status
LET01160 In distribution
LET01255 In distribution
LET81150 In distribution
LET00955 In distribution
LET01140 In distribution
LET81160 In distribution
LET80950 In distribution
LET71245 In distribution
LET71560 In distribution
LET01250 In distribution
LET71145 In distribution
LET01260 In distribution
LET80940 In distribution
LET01355 In distribution
LET71550 In distribution
LET71545 In distribution
LET81450 In distribution
LET01450 In distribution
LET01645 In distribution
LET71250 In distribution
LET81145 In distribution
LET81245 In distribution
LET71160 In distribution
LET01440 In distribution
LET80945 In distribution
LET71345 In distribution
LET81550 In distribution
LET01055 In distribution
LET71650 In distribution
LET81055 In distribution
LET81455 In distribution
LET01545 In distribution
LET71355 In distribution
LET81060 In distribution
LET81540 In distribution
LET00855 In distribution
LET01050 In distribution
LET71055 In distribution
LET81645 In distribution
LET81545 In distribution
LET71150 In distribution
LET01560 In distribution
LET71450 In distribution
LET00840 In distribution
LET81660 In distribution
LET80850 In distribution
LET80955 In distribution
LET01360 In distribution
LET01045 In distribution
LET81460 In distribution
LET81045 In distribution
LET00950 In distribution
LET71460 In distribution
LET81340 In distribution
LET01245 In distribution
LET00850 In distribution
LET01650 In distribution
LET71555 In distribution
LET71040 In distribution
LET80845 In distribution
LET71655 In distribution
LET01445 In distribution
LET71050 In distribution
LET81350 In distribution
LET01460 In distribution
LET80860 In distribution
LET71255 In distribution
LET01550 In distribution
LET01555 In distribution
LET81140 In distribution
LET01060 In distribution
LET01040 In distribution
LET81650 In distribution
LET71445 In distribution
LET81155 In distribution
LET71440 In distribution
LET71155 In distribution
LET81040 In distribution
LET81250 In distribution
LET81560 In distribution
LET71660 In distribution
LET81440 In distribution
LET01455 In distribution
LET81640 In distribution
LET01340 In distribution
LET01240 In distribution
LET81655 In distribution
LET01350 In distribution
LET81345 In distribution
LET01660 In distribution
LET71340 In distribution
LET71240 In distribution
LET01640 In distribution
LET01155 In distribution
LET81050 In distribution
LET01150 In distribution
LET00860 In distribution
LET81260 In distribution
LET01655 In distribution
LET81255 In distribution
LET81555 In distribution
LET00845 In distribution
LET71455 In distribution
LET00960 In distribution
LET71060 In distribution
LET80855 In distribution
LET71640 In distribution
LET71045 In distribution
LET71140 In distribution
LET01145 In distribution
LET81445 In distribution
LET00940 In distribution
LET71360 In distribution
LET71260 In distribution
LET81360 In distribution
LET80960 In distribution
LET01345 In distribution
LET00945 In distribution
LET81355 In distribution
LET71350 In distribution
LET80840 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
K201605 2020-07-15
K183447 2019-02-04
K181644 2018-10-12
K172888 2017-12-15
K170503 2017-07-11

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