Skytron Front Rail 10″

Front Equip. Rail 10"

Registry build 21.09.26
11manufacturers in China registered for this device type
1catalogue number
7recalls on this code

Who Else Makes It

Concentrated in Jiangsu (6), Shanghai (1), Anhui (1).

Chinese manufacturers registered for FDA product code FQO
Manufacturer City Province Registered as Device types
Jiangsu Saikang Medical Equipment Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 34
Jiangsu Yongfa Medical Equipment Technology Co., Ltd. Zhangjiagang Jiangsu Manufacturer 33
Shanghai NO. 2 Medical College Duhang Medical Equipment Factory Shanghai Shanghai Contract manufacturer 32
Jiangsu Rooe Medical Technology Co., Ltd. Zhangjiagang Jiangsu Manufacturer 31
Hefei MT Medical Co., Ltd. Hefei Anhui Manufacturer 23
Jiangsu Keling Medical Appliances Co., Ltd. Yangzhou Jiangsu Contract manufacturer 23
Hebei Jiede Medical Equipment Co., Ltd. Hengshui Hebei Contract manufacturer 20
Suzhou Number WIN Medical Technology Co., Ltd. Zhangjiagang Jiangsu Manufacturer 16
Shandong Deman Medical Equipment Group Co., Ltd. Jining Shandong Manufacturer 11
Nanchang Micare Medical Equipment Co., Ltd. Nanchang Jiangxi Manufacturer 8
Nanjing Mindray BIO-Medical Electronics Co., Ltd. Nanjing Jiangsu Manufacturer 2

Record

Regulatory record for Skytron front rail 10″
Listed by Skytron, LLC, United States
FDA product code FQO
Device type Table, Operating-Room, Ac-Powered
Device class Class 1
Regulation 21 CFR 878.4960
Establishment Specification developer, Complaint-file establishment, Manufacturer
Premarket notification Exempt
Record published 2019-04-30

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only

Catalogue Numbers

Catalogue numbers for Skytron front rail 10″
Catalogue number Size Status
H8-300-08 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
HarmonyAIR Steris Corporation 452
Skytron Skytron, LLC 200
Table, Operating-Room, Ac-Powered Steris Corporation 165
iCE boom and Pendant Amico Clinical Solutions 102
Mindray Nanjing Mindray BIO-Medical Electronics Co., Ltd. 95
Amtai Amtai Medical Equipment, Inc. 95
Steris Steris Corporation 72
Alyon Steris Corporation 41
Foot switch Maquet Gmbh 23
Amsco Steris Corporation 14
Atec A.R.M. Alphatec Spine, Inc. 13
Universal table top Maquet Gmbh 13

Showing 12 of 442. All products under Table, Operating-Room, Ac-Powered

Recalls

5 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2022-06-02 Class II Component design/selection Under certain circumstances, the mounting screws may loosen or pull out from the attachment point on the Ergon 3 boom when the GCX Channel Mounting Accessory was used with the VST clamp as a monitor mount on the boom. 731
2021-05-11 Class II Device Design Failure of the FS32 Monitor Brackets from the mounting block could potentially loosen over time and eventually detach from the baseplate, result in the display interface dismounting from its attachment point, causing injury to patients or s 278 units US; 7 units OUS
2020-03-05 Class II Device Design Potential for the weld to fail at the pivot point of the monitor bracket. This weld failure could cause the display interface and bracket to fall from its mounted location, resulting in injury. 43 units
2016-03-28 Class II Process design Potential for the weld to fail at the pivot point of the monitor bracket. This weld failure could cause the display interface and bracket to fall from its mounted location, resulting in injury. 24 2017-07-25
2015-12-02 Class II Device Design The hardware that holds the VESA plate and the display interface / monitor to the bracket may fail causing the display interface to fall from the bracket. Over time and with use the threaded rod hardware material can weaken and detach from 286 2016-07-19
2005-08-04 Not classified Other The release levers can inadvertently release under load while the leg section is positioned at a ninety degree angle causing the leg section to drop. 160 total 2008-05-01
2005-08-04 Not classified Other The release levers can inadvertently release under load while the leg section is positioned at a ninety degree angle causing the leg section to drop. 160 total 2008-05-01

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