Vocsn-VC

VOCSN-VC provides mechanical ventilation and cough assistance in one portable system. Its ventilation function supports pediatric and adult patients weighing at least 5 kg, using invasive…

Registry build 21.09.26

VOCSN-VC provides mechanical ventilation and cough assistance in one portable system. Its ventilation function supports pediatric and adult patients weighing at least 5 kg, using invasive or noninvasive interfaces. It is intended for home, hospital, institutional and transport settings.

A microprocessor controls a radial blower, valves and sensors to deliver positive-pressure breaths. For cough assistance, the system applies positive airway pressure followed by a rapid change to negative pressure. This generates expiratory flow to help patients who cannot cough or clear secretions effectively.

Listed Item

VOCSN-VC Pro, English: The VC configuration of VOCSN contains Ventilation and Cough therapies. The VOCSN Unified Respiratory System is intended to provide continuous or intermittent ventilatory support for the care of individuals who require mechanical ventilation. It may be used in invasive and non-invasive applications. The VOCSN is intended for pediatric through adult patients weighing at least 5 kg. It is intended for use in home, hospital, institutional and transport settings, including portable applications. The integral cough assist option is intended for patients who are additionally unable to cough or clear secretions effectively. www.VentecLife.com

Power and Controls

The system can run from AC power, DC power or internal batteries. A central interface sets therapy controls and displays monitoring information, with alarms to alert users to hazardous conditions.

8manufacturers in China registered for this device type
1catalogue number
1510(k) clearance
4recalls on this code

Who Else Makes It

Concentrated in Guangdong (4), Jiangsu (2), Fujian (1). 6 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code CBK
Manufacturer City Province Registered as Device types
GaleMed (Xiamen) Co., Ltd. Xiamen Fujian Contract manufacturer 33
Vincent Medical (Dong Guan) Manufacturing Co., Ltd. Dong Guan Guangdong Contract manufacturer 29
Sanmina Kunshan Jiangsu Contract manufacturer 15
Mehow Innovative (Huizhou) Ltd. Huizhou Guangdong Contract manufacturer 11
Respironics Medical Products (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 8
Beijing Aeonmed Co., Ltd. Sanhe Hebei Contract manufacturer 7
Shenzhen Mindray BIO-Medical Electronics Co., Ltd. Shenzhen Guangdong Specification developer 61
GE Medical Systems (China) Co., Ltd. Wuxi Jiangsu Contract manufacturer 57

Record

Regulatory record for Vocsn-VC
Listed by Ventec Life Systems, Inc., United States
FDA product code CBK
Device type Ventilator, Continuous, Facility Use
Device class Class 2
Regulation 21 CFR 868.5895
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K162877
Record published 2019-01-30
Record revised 2025-12-10 (version 3)

Specifications

Specifications
MRI safety MR Unsafe
Prescription Prescription only
Latex Labelled latex-free
Label carries manufacturing date, serial number
Storage Storage environment temperature -25 to 70 °C; Storage environment humidity 0 to 90 % RH; Storage environment atmospheric pressure 50 to 110 KiloPascal

Catalogue Numbers

Catalogue numbers for Vocsn-VC
Catalogue number Size Status
VOCSN-VC Pro, English In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Puritan Bennett Covidien LP 285
Newport Newport Medical Instruments, Inc. 103
LTV Vyaire Medical, Inc. 92
Ventilator, Continuous, Facility Use Hans Rudolph, Inc. 66
Infant Flow SiPAP Carefusion 62
Avea Carefusion 57
Ventoux Flight Medical Innovations Ltd. 48
Trilogy Respironics Inc. 42
Avea™ Vyaire Medical, Inc. 39
Patient Circuits Zoll Medical Corporation 38
Performatrak Respironics Inc. 35
Bio-Med Devices, Inc. BIO-MED Devices, Inc. 34

Showing 12 of 419. All products under Ventilator, Continuous, Facility Use

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K162877 2017-04-07

Recalls Naming This Product

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

Recalls naming the identifiers of Vocsn-VC
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Ventec Life Systems, Inc. 510(k) number 2026-05-08 Class II Vendor change control Respiratory system intended to provide continuous/intermittent ventilator support, may have a damaged back-up battery supporting backup alarm function, which may result in the backup alarm not activating during loss of primary power and abs 1
Ventec Life Systems, Inc. 510(k) number 2026-03-25 Class I Process change control Respiratory system intended to provide continuous/intermittent ventilator support, may not have been evaluated under all intended high-pressure conditions during production testing, so an oxygen leak condition could occur that may lead to r 42
Ventec Life Systems, Inc. 510(k) number 2025-02-03 Class I Component change control Multi-Function Ventilators were serviced using incorrect parts which have the potential to cause unexpected shutdown, or when using an active circuit could result in inaccurate tidal volume monitor, not triggering on patient efforts, less i 30
Ventec Life Systems, Inc. 510(k) number 2024-01-09 Class I Process control The bonded spiral wrap may detach before or during ventilation due to a manufacturing issue. Detachment of the spiral wrap can compromise structural integrity, functionality and/ or performance resulting in occlusions or leaks of the breat 250 breathing circuits
Ventec Life Systems, Inc. 510(k) number 2021-05-10 Class II Device Design Due to a component failure, ventilators may unexpectedly shut down or have a loss of blower function while in patient use. The shutdown potentially prevents the ventilator from providing ventilation therapy. 1,934 devices (415 device that have not been updated)

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