Steris

The STERIS 4085 Table Battery Line ABS Featherweight Leg Section with TLT Pads accommodates virtually all patients with generous weight and height ranges and provides outstanding access for…

Registry build 21.09.26

The STERIS 4085 Table Battery Line ABS Featherweight Leg Section with TLT Pads accommodates virtually all patients with generous weight and height ranges and provides outstanding access for C-Arm, permitting high quality images crucial to cardiothoracic, Orthopedic and neurosurgical procedures.

11manufacturers in China registered for this device type
72catalogue numbers in this listing
2510(k) clearances naming this product code
6recalls 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 Steris
Listed by Steris Corporation, United States
FDA product code FQO
Device type Table, Operating-Room, Ac-Powered
Device class Class 1
Regulation 21 CFR 878.4960
Establishment Contract manufacturer, Contract steriliser, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K090136
Record published 2023-11-17
Record revised 2026-04-30 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Over the counter Yes
Label carries manufacturing date, serial number
Distribution end date 2026-07-22

Catalogue Numbers

Catalogue numbers for Steris
Catalogue number Size Status
4095 Surigical Table In distribution
4095 Surigical Table In distribution
5085 SRT Surgical Table In distribution
5095 Surigical Table In distribution
4095 Surigical Table In distribution
5085 SRT Surgical Table In distribution
4095 Surigical Table In distribution
5095 Surigical Table In distribution
4095 Surigical Table In distribution
5095 Surgical Table In distribution
5095 Surigical Table In distribution
4095 Surigical Table In distribution
4095 Surgical Table In distribution
5095 Surigical Table In distribution
4095 Surigical Table In distribution
4095 Surigical Table In distribution
4095 Surigical Table In distribution
4095 Surigical Table In distribution
5085 SRT Surgical Table In distribution
5085 SRT Surgical Table In distribution
5095 Surigical Table In distribution
4095 Surigical Table In distribution
5085 SRT Surgical Table In distribution
5085 SRT Surgical Table In distribution
4095 Surgical Table Withdrawn
4095 Surigical Table Withdrawn
4085 Surgical Table Withdrawn
5085 Surgical Table Withdrawn
4095 Surigical Table Withdrawn
4095 Surigical Table Withdrawn
4095 Surigical Table Withdrawn
4085 Surgical Table Withdrawn
4085 Surgical Table Withdrawn
4095 Surgical Table Withdrawn
5085 Surgical Table Withdrawn
5095 Surigical Table Withdrawn
5085 Surgical Table Withdrawn
5095 Surigical Table Withdrawn
5085 SRT Surgical Table Withdrawn
4085 Surgical Table Withdrawn
4085 Surgical Table Withdrawn
4085 Surgical Table Withdrawn
4085 Surgical Table Withdrawn
5085 Surgical Table Withdrawn
5085 SRT Surgical Table Withdrawn
5085 Surgical Table Withdrawn
4085 Surgical Table Withdrawn
5085 Surgical Table Withdrawn
5085 Surgical Table Withdrawn
4095 Surigical Table Withdrawn
5085 Surgical Table Withdrawn
5085 Harmony Surgical Table Withdrawn
5085 SRT Surgical Table Withdrawn
4085 Surgical Table Withdrawn
5085 Harmony Surgical Table Withdrawn
5085 Surgical Table Withdrawn
4085 Surgical Table Withdrawn
4085 Surgical Table Withdrawn
5095 Surgical Table Withdrawn
5085 Surgical Table Withdrawn
4095 Surigical Table Withdrawn
5095 Surigical Table Withdrawn
4095 Surigical Table Withdrawn
5095 Surigical Table Withdrawn
5085 SRT Surgical Table Withdrawn
5085 Surgical Table Withdrawn
5085 SRT Surgical Table Withdrawn
4095 Surigical Table Withdrawn
5085 SRT Surgical Table Withdrawn
5085 SRT Surgical Table Withdrawn
4085 Surgical Table Withdrawn
5085 Surgical Table Withdrawn

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
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
Magnus operating table system Maquet Gmbh 8

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

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K090136 2009-03-20
K971307 1997-06-27

Recalls Naming This Product

2 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of Steris
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Steris Corporation 510(k) number 2011-10-17 Not classified Nonconforming Material/Component Some hydraulic column cylinders installed in certain 5085 and 5085SRT Surgical Tables were assembled by their supplier with incorrect snap rings and an anomaly was present in the tilt cylinder. This error may affect the user’s ability to mo 167 tables were distributed – 5085=108 and 5085SRT=59 2013-03-19
Steris Corporation 510(k) number 2010-05-14 Not classified Nonconforming Material/Component STERIS has learned that a limited quantity of manifold assemblies were manufactured by our supplier with incorrect washers and springs in the valves of the manifold. This supplier error has the potential to cause: a) an inability to articu 79 units 2012-02-24

Recalls

2 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
2014-06-27 Class II Device Design STERIS engineering analysis has determined the D1 pressure switch in the hydraulic column manifold does not adequately detect pressure level. If one or more of the table floor lock feet become unlocked due to the loss of hydraulic pressur 3689 2015-09-16
2010-08-12 Not classified Other Cmax Surgical Tables may lose calibration if the table is operated only on battery power and if the table is in a low battery charge condition. This could result in the table moving into an unexpected tilt position when the Level button is 1,635 tables 2012-09-27
2010-02-17 Class II Employee error Customers may be storing objects on the base and/or around the column of the surgical table. This prohibited practice and misuse known by the customers can damage the override switch assembly located at the top of the column cover. Depend 11,044 Units 2013-03-13
2009-05-12 Not classified Process control A limited quantity of the Cmax Hand Controls, P150832-500, were manufactured without Loctite thread locker on the screws that attach the mounting clip to the hand control case. This clip provides a means of storing the hand control on the 217 Units 2013-02-26

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