Data / Medical devices / China / Zhongshan A&j Medical Equipment Co., Ltd.
Zhongshan A&j Medical Equipment Co., Ltd.: FDA-registered device maker in Guangdong, China, 3 510(k) clearances
Zhongshan A&j Medical Equipment Co., Ltd. is registered with the FDA (registration 3004443928) in Guangdong, China. It lists 7 device types. The FDA files 3 510(k) clearances under its listings, the newest dated June 26, 2007. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3004443928
- Address
- 3 Shenghui South Road Nantou Town, Zhongshan City, Guangdong, China, --
- Owner or operator
- TAIWAN AN I CO.,LTD. (9021165)
- Roles
- Manufacturer
- First device listed
- March 27, 2002
- Registered through
- 2026
- Brand names listed
- AMG USA, Airgo, Alevo, Breezy, Disposable Splint, Drive, EVEREST JENNINGS, Feather and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Chair, With Casters | INM | 1 | Manufacturer | accessdata.fda.gov |
| Nebulizer (Direct Patient Interface) | CAF | 2 | Manufacturer | accessdata.fda.gov |
| Pump, Portable, Aspiration (Manual Or Powered) | BTA | 2 | Manufacturer | accessdata.fda.gov |
| Splint, Extremity, Non-Inflatable, External, Non-Sterile | NOC | 1 | Manufacturer | accessdata.fda.gov |
| Stretcher, Hand-Carried | FPP | 1 | Manufacturer | accessdata.fda.gov |
| Walker, Mechanical | ITJ | 1 | Manufacturer | accessdata.fda.gov |
| Wheelchair, Powered | ITI | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| June 26, 2007 | K071607 | ASA01 HEAVY DUTY SUCTION PUMP | BTA | Substantially Equivalent | Zhongshan A&J Medical Equipment Co., Ltd. | accessdata.fda.gov |
| December 21, 2005 | K052811 | HSINER JET NEBULIZER, MODEL HS-31100 | CAF | Substantially Equivalent | Hsiner Co., Ltd. | accessdata.fda.gov |
| May 25, 2004 | K041190 | A&I POWER WHEELCHAIR, PC-401 | ITI | Substantially Equivalent | Well Success Biotech, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Splint, Extremity, Non-Inflatable, External, Non-Sterile
- All makers of Nebulizer (Direct Patient Interface)
- All makers of Pump, Portable, Aspiration (Manual Or Powered)
- All makers of Walker, Mechanical
- All makers of Chair, With Casters
- All makers of Stretcher, Hand-Carried
Updated June 26, 2007. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.