Arya

Arya Portable Oxygen Concentrator, with autoSAT function 4 btn. Does not include power supply, portable concentrator only

Registry build 21.09.26
22manufacturers in China registered for this device type
9catalogue numbers in this listing
4510(k) clearances naming this product code
7recalls on this code

Who Else Makes It

Concentrated in Jiangsu (6), Guangdong (5), Beijing (2). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code CAW
Manufacturer City Province Registered as Device types
Foshan Kycare Medical Equipment Co., Ltd. Foshan Guangdong Contract manufacturer 3
Jakamed Instruments Co., Ltd. Changsha Hunan Contract manufacturer 2
Jiangsu Jumao X-Care Medical Equipment Co., Ltd. Danyang Jiangsu Contract manufacturer 37
Beijing Choice Electronic Technololgy Co., Ltd. Beijing Beijing Repacker / relabeller 30
Jiangsu Yuyue Medical Equipment & Supply Company Limited Jiangsu Jiangsu Contract manufacturer 17
Tianjin Choice Medical Device Co., Ltd. Tianjin Tianjin Contract manufacturer 12
Danyang Huayi Medical Supply & Equipment Co., Ltd. Danyang Jiangsu Contract manufacturer 11
Shandong Moonlight Electronics Tech Co., Ltd. Weifang Shandong Manufacturer 11
Honsun (Nantong) Co., Ltd. Nantong Jiangsu Contract manufacturer 9
Beijing Choicemmed Technology Co., Ltd. Beijing Beijing Repacker / relabeller 9
Foshan Care Medical Technology Co., Ltd. Foshan Guangdong Manufacturer 3
Zhengzhou Olive Electronic Technology Co., Ltd. Zhengzhou Henan Manufacturer 3

Showing 12 of 22. All 22 manufacturers in China registered for Generator, Oxygen, Portable

Record

Regulatory record for Arya
Listed by Caire Inc., United States
FDA product code CAW
Device type Generator, Oxygen, Portable
Device class Class 2
Regulation 21 CFR 868.5440
Establishment Specification developer, Repacker / relabeller, Manufacturer
510(k) K020324
Record published 2021-11-08

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries manufacturing date, serial number
Storage Handling environment temperature 41 to 104 °F

Catalogue Numbers

Catalogue numbers for Arya
Catalogue number Size Status
AS200-6 In distribution
AS200-6R In distribution
AS200-SW6 In distribution
AS200-206 In distribution
AS200-46 In distribution
AS200-146 In distribution
AS200-106 In distribution
AS200-246 In distribution
AS200-SW46 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
DeVilbiss DeVilbiss Healthcare LLC. 50
EverFlo Respironics Inc. 32
Mark 5 Nuvo Lite Nidek Medical Products, Inc. 30
SimplyGo Mini Respironics Inc. 26
X-PLO2R Belluscura, LLC 17
Mark 5 Nuvo 8 Nidek Medical Products, Inc. 12
ViveBreathe Vive Health LLC 11
Invacare® HomeFill® Oxygen System Invacare GmbH 11
Discov-R Belluscura, LLC 11
NewLife Elite Caire Inc. 10
NewLife Elite Airsep Corp. 10
Rhythm Healthcare Qingdao Kingon Medical Science AND Technology Co., Ltd. 9

Showing 12 of 187. All products under Generator, Oxygen, Portable

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K250671 2025-07-11
K120785 2012-10-25
K121167 2012-05-02
K952268 1995-08-11

Recalls Naming This Product

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

Recalls naming the identifiers of Arya
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Caire Inc. 510(k) number 2024-10-04 Class II Nonconforming Material/Component Potential failure of affected units to recharge the battery of the oxygen concentrators. 739 concentrators
Caire Inc. 510(k) number 2024-10-04 Class II Nonconforming Material/Component Potential failure of affected units to recharge the battery of the oxygen concentrators. 23 concentrators
Oxus America, Inc. 510(k) number 2013-01-14 Class II Nonconforming Material/Component Due to past battery inventory storage conditions and deficiencies in the maintenance procedure, it was possible that some batteries were over-discharged to point of damaging the cells. 1724 total units 2013-07-17

Recalls

5 of these are Class II. Class II means a temporary or reversible health consequence. 1 is recorded with the root cause “No Marketing Application”: the device was distributed without the premarket submission its class requires, a compliance finding rather than a defect. 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
2024-10-04 Class II Nonconforming Material/Component Potential failure of affected units to recharge the battery of the oxygen concentrators. 26 concentrators
2024-10-04 Class II Nonconforming Material/Component Potential failure of affected units to recharge the battery of the oxygen concentrators. 6 concentrators
2022-03-25 Class II No Marketing Application The device was not cleared for U.S. distribution. 2 oxygen concentrators 2023-10-05
2019-11-21 Class II Packaging process control Four units of European version FreeStyle Comfort were distributed in the US, but were not cleared for use in the US.. 4 units 2020-11-20
2019-09-16 Class II Nonconforming Material/Component There is an electronics control issue that causes the unit to not power on with battery power only. 10 units 2020-12-16

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