Vanguard® SSK Revision

Catalogue number 32-488512, listed by Biomet Orthopedics, United States, under Chisel, Surgical, Manual. 10 manufacturers in China are registered for this product code.

Registry build 21.09.26
10manufacturers in China registered for this device type
1catalogue number

Who Else Makes It

Concentrated in Shanghai (3), Zhejiang (3), Jiangsu (3). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code FZO
Manufacturer City Province Registered as Device types
Canwell Medical Co., Ltd. Jinhua Zhejiang Contract manufacturer 42
B.Braun Medical (Suzhou) Co,.Ltd Suzhou Jiangsu Contract manufacturer 37
Suzhou Microport Orthorecon Co., Ltd. Suzhou Jiangsu Contract manufacturer 31
Shanghai KiNETIC Medical Co Ltd Shanghai Shanghai Contract manufacturer 19
Shanghai Medical Instruments (Group) Ltd. Corp. Shanghai Shanghai Contract manufacturer 235
Xinhua Surgical Instrument Co., Ltd. Zibo Shandong Manufacturer 222
MicroPort Orthopedics Global Supply Center Limited Shanghai Shanghai Contract manufacturer 82
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Tonglu Wanhe Medical Instrument Co., Ltd. Hangzhou Zhejiang Manufacturer 24

Record

Regulatory record for Vanguard® SSK Revision
Listed by Biomet Orthopedics, United States
FDA product code FZO
Device type Chisel, Surgical, Manual
Device class Class 1
Regulation 21 CFR 878.4800
Premarket notification Exempt
Record published 2022-05-08
Record revised 2025-05-30 (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

Catalogue Numbers

Catalogue numbers for Vanguard® SSK Revision
Catalogue number Size Status
32-488512 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Surtex Surtex Instruments Ltd 297
Sklar Sklar Corporation 175
Medicon Medicon eG. Chirurgiemechaniker-Genossenschaft 119
Timberline Lateral Fusion System Highridge Medical, LLC 96
Ambler Surgical Ambler Surgical, LLC 95
RZ Medizintechnik GmbH RZ Medizintechnik Gmbh 87
Integra® Jarit® Integra LifeSciences Production Corporation 60
Boss Instruments Boss Instruments, Ltd. 52
Integra® Miltex® Integra LifeSciences Production Corporation 50
Aesculap Aesculap AG 42
Kmedic Teleflex Medical LLC 41
American Medicals American Medicals 41

Showing 12 of 179. All products under Chisel, Surgical, Manual

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