ReLine

RELINE-C Conn, 3.5x4.0mm Offset Open Top

Registry build 21.09.26
4manufacturers in China registered for this device type
1,072catalogue numbers in this listing

Who Else Makes It

Concentrated in Jiangsu (1), Shandong (1), Fujian (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code NKG
Manufacturer City Province Registered as Device types
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Double Medical Technology Inc. Xiamen Fujian Contract manufacturer 14
Zhejiang Decans Medical Devices Co., Ltd. Jiaxing Zhejiang Manufacturer 10

Record

Regulatory record for ReLine
Listed by Nuvasive, Inc., United States
FDA product code NKG
Device type Posterior Cervical Screw System
Device class Class 2
Regulation 21 CFR 888.3075
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K191553
Record published 2019-12-10
Record revised 2025-11-20 (version 5)

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

Catalogue Numbers

Catalogue numbers for ReLine
Catalogue number Size Status
3744055 In distribution
3704510 In distribution
3786548 In distribution
3734546 In distribution
3924026 In distribution
3700314 In distribution
3749502 In distribution
3736030 In distribution
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3814010 In distribution
3764534 In distribution
3737535 In distribution
3735025 In distribution
3736044 In distribution
3700304 In distribution
3841450 In distribution
3776558 In distribution
3913542 In distribution
3965328 In distribution
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3836552 In distribution
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3841080 In distribution
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3763522 In distribution
3835538 In distribution
3843105 In distribution
3903510 In distribution
3736548 In distribution
3935025 In distribution
3804034 In distribution
3764038 In distribution
3786526 In distribution

Showing 250 of 300 catalogue numbers.

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Bridalveil Astura Medical 1,718
Proficient™ Posterior Cervical Spine System Spine Wave, Inc. 1,590
Invictus Alphatec Spine, Inc. 1,538
Paeon Posterior Cervical Fixation System Aegis Spine 1,408
PathLoc-C Posterior Cervical Fixation System L&K Biomed Co., Ltd. 706
Cosy Signus Medizintechnik Gmbh 550
Yukon OCT Spinal System VB Spine LLC 451
Astra-OCT Spine System Spinecraft LLC 440
Symphony Medos International Sàrl 389
Medyssey Poseidon OCT Spinal Fixation System Medyssey Co., Ltd. 387
Infinity™ Occipitocervical Upper Thoracic System Medtronic Sofamor Danek, Inc. 375
Perla ® Spineart SA 349

Showing 12 of 336. All products under Posterior Cervical Screw System

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