Timberline Lateral Fusion System

Solid WEB Rotating Disc Cutter 14MM

Registry build 21.09.26
17manufacturers in China registered for this device type
46catalogue numbers in this listing

Who Else Makes It

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

Chinese manufacturers registered for FDA product code FZT
Manufacturer City Province Registered as Device types
Xinhua Healthcare Industry Co., Limited Zibo Shandong Contract manufacturer 30
Mobility Source Medical Technology Co., Ltd. Foshan Guangdong Contract manufacturer 26
Boen Healthcare Co., Ltd. Suzhou Jiangsu Specification developer 263
Shanghai Medical Instruments (Group) Ltd. Corp. Shanghai Shanghai Contract manufacturer 235
MicroPort Orthopedics Global Supply Center Limited Shanghai Shanghai Contract manufacturer 82
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Bothwin (Beijing) Medical Technology Co., Ltd. Beijng Beijing Manufacturer 25
Guangdong Shunde LQX Health Technology Inc. Foshan Guangdong Contract manufacturer 24
Tonglu Wanhe Medical Instrument Co., Ltd. Hangzhou Zhejiang Manufacturer 24
Taizhou Rich Medical Products Co., Ltd. Taizhou Jiangsu Contract manufacturer 20
Foshan Coxo Medical Instrument Co., Ltd. Foshan Guangdong Manufacturer 19
Ningbo Huakun Medical Equipment Co., Ltd. Cixi Zhejiang Contract manufacturer 19

Showing 12 of 17. All 17 manufacturers in China registered for Cutter, Surgical

Record

Regulatory record for Timberline Lateral Fusion System
Listed by Highridge Medical, LLC, United States
FDA product code FZT
Device type Cutter, Surgical
Device class Class 1
Regulation 21 CFR 878.4800
Establishment Specification developer, Manufacturer
Premarket notification Exempt
Record published 2025-12-16

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization

Catalogue Numbers

Catalogue numbers for Timberline Lateral Fusion System
Catalogue number Size Status
8738-5409 In distribution
8738-5408 In distribution
8738-5415 In distribution
8732-5415 In distribution
8738-5417 In distribution
8738-5410 In distribution
8732-5409 In distribution
8732-5414 In distribution
8732-5420 In distribution
8732-5417 In distribution
8732-5418 In distribution
8738-5419 In distribution
8738-5412 In distribution
8738-1001 In distribution
8738-5314 In distribution
8738-5407 In distribution
8738-5313 In distribution
8738-5306 In distribution
8732-5419 In distribution
8738-5420 In distribution
8732-5413 In distribution
8732-5412 In distribution
8738-5416 In distribution
8738-5312 In distribution
8738-5413 In distribution
8738-5418 In distribution
8738-5318 In distribution
8732-5416 In distribution
8738-5310 In distribution
8738-5317 In distribution
8732-5407 In distribution
8732-5411 In distribution
8732-5410 In distribution
8738-5406 In distribution
8732-5408 In distribution
8738-5315 In distribution
8738-5309 In distribution
8738-5320 In distribution
8738-5316 In distribution
8738-5319 In distribution
8738-5414 In distribution
8738-5308 In distribution
8738-5307 In distribution
8738-5411 In distribution
8732-5406 In distribution
8738-5311 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Medtronic Reusable Instruments Medtronic Sofamor Danek, Inc. 326
Sklar® Sklar Corporation 93
Tecomet Tecomet, Inc. 89
Aesculap Aesculap AG 38
Orthomed Ortho-MED, Inc. 37
Surtex Surtex Instruments Ltd 35
SeaSpine Spacer System – Pacifica Seaspine Orthopedics Corporation 24
Millennium Avalign Technologies, Inc. 23
Cutter, Surgical Medtronic Sofamor Danek, Inc. 22
Medtronic Resuable Instruments Medtronic Sofamor Danek, Inc. 22
Velofix™ PEEK Lumbar Cage CG MedTech Co., Ltd. 20
Skyhawk Orthofix US LLC 19

Showing 12 of 177. All products under Cutter, Surgical

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