SEA-Link Anterior Cervical Plate System

SEA-LINK Anterior Cervical Plate System Three Level Plate 54 mm

Registry build 21.09.26
14manufacturers in China registered for this device type
30catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Jiangsu (5), Shanghai (3), Zhejiang (2). 8 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code KWQ
Manufacturer City Province Registered as Device types
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
APS Materials Suzhou Suzhou Jiangsu Contract manufacturer 18
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Johnson & Johnson Medical (Depuy – Suzhou) Ltd. Suzhou Jiangsu Manufacturer 34
Double Medical Technology Inc. Xiamen Fujian Contract manufacturer 14

Showing 12 of 14. All 14 manufacturers in China registered for Appliance, Fixation, Spinal Intervertebral Body

Record

Regulatory record for SEA-Link Anterior Cervical Plate System
Listed by Indius Medical Technologies PVT. Ltd., India
FDA product code KWQ
Device type Appliance, Fixation, Spinal Intervertebral Body
Device class Class 2
Regulation 21 CFR 888.3060
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer
Record published 2021-01-20
Record revised 2025-11-20 (version 3)

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 19 to 97 mm

Catalogue Numbers

Catalogue numbers for SEA-Link Anterior Cervical Plate System
Catalogue number Size Status
A003.0123 Length 23 mm In distribution
A003.0481 Length 81 mm In distribution
A003.0354 Length 54 mm In distribution
A003.0497 Length 97 mm In distribution
A003.0363 Length 63 mm In distribution
A003.0121 Length 21 mm In distribution
A003.0493 Length 93 mm In distribution
A003.0485 Length 85 mm In distribution
A003.0254 Length 54 mm In distribution
A003.0357 Length 57 mm In distribution
A003.0243 Length 43 mm In distribution
A003.0473 Length 73 mm In distribution
A003.0477 Length 77 mm In distribution
A003.0119 Length 19 mm In distribution
A003.0241 Length 41 mm In distribution
A003.0131 Length 31 mm In distribution
A003.0469 Length 69 mm In distribution
A003.0366 Length 66 mm In distribution
A003.0125 Length 25 mm In distribution
A003.0360 Length 60 mm In distribution
A003.0127 Length 27 mm In distribution
A003.0251 Length 51 mm In distribution
A003.0233 Length 33 mm In distribution
A003.0245 Length 45 mm In distribution
A003.0237 Length 37 mm In distribution
A003.0248 Length 48 mm In distribution
A003.0489 Length 89 mm In distribution
A003.0239 Length 39 mm In distribution
A003.0129 Length 29 mm In distribution
A003.0235 Length 35 mm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
ReLine Nuvasive, Inc. 2,998
CD Horizon® Spinal System Medtronic Sofamor Danek, Inc. 2,568
Creo Globus Medical, Inc. 1,765
AccelFix Spinal Fixation System L&K Biomed Co., Ltd. 1,755
Ozark Cervical Plate System VB Spine LLC 1,460
Sirion Astura Medical 1,246
Apex Spine System Spinecraft LLC 1,187
AnyPlus Spinal Fixation System GS Medical Co., Ltd. 986
Astra Spine System Spinecraft LLC 970
Zavation Zavation 966
ACP Nuvasive, Inc. 918
Polaris™ 5.5 Spinal System Biomet Spine 877

Showing 12 of 855. All products under Appliance, Fixation, Spinal Intervertebral Body

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K200224 2020-03-24

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