Mojo 2 Full Face Non Vented Mask, Large

4 catalogue numbers from 50914, listed by Sleepnet Corporation, United States, under Ventilator, Continuous, Facility Use. 8 manufacturers in China are registered for this product code.

Registry build 21.09.26
8manufacturers in China registered for this device type
4catalogue numbers in this listing
4510(k) clearances naming this product 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 Mojo 2 Full Face Non Vented Mask, Large
Listed by Sleepnet Corporation, United States
FDA product code CBK
Device type Ventilator, Continuous, Facility Use
Device class Class 2
Regulation 21 CFR 868.5895
Establishment Manufacturer, Exporter
Record published 2019-05-03
Record revised 2019-12-13 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number, expiry date, manufacturing date
Storage Storage environment temperature up to 122 °F

Catalogue Numbers

Catalogue numbers for Mojo 2 Full Face Non Vented Mask, Large
Catalogue number Size Status
50914 In distribution
50914 In distribution
50914 In distribution
50914 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
K241943 2024-08-28
K241520 2024-06-27
K190533 2019-07-26
K063806 2007-05-17

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