Data / Medical devices / China / Dongguan Aidisy Machinery & Electronic Equipment Co., Ltd.
Dongguan Aidisy Machinery & Electronic Equipment Co., Ltd.: FDA-registered device maker in Dongguan Guangdong, China, 1 510(k) clearance
Dongguan Aidisy Machinery & Electronic Equipment Co., Ltd. is registered with the FDA (registration 3011189029) in Dongguan Guangdong, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 19, 2013. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3011189029
- Address
- Part B,3rd F, Block A, Wentang Industrial Park,Longhua Road,Zhouwu Dongcheng District Dongguan City,Guangdong Province,523000, P.R.China., Dongguan Guangdong, China, 523000
- Owner or operator
- Dongguan Aidisy Machinery & Electronic Equipment Co., Ltd. (10047031)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- June 16, 2014
- Registered through
- 2026
- Brand names listed
- Clever Choice, NEBULIZER, PMI Probasics Nebulizer
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Nebulizer (Direct Patient Interface) | CAF | 2 | Exporter to the US, 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 |
|---|---|---|---|---|---|---|
| December 19, 2013 | K123030 | COMPRESSOR NEBULIZER MODEL MCN-S600XX | CAF | Substantially Equivalent | Dongguan Aidisy Machinery & Electronic Equipment C | accessdata.fda.gov |
Compare with other makers
Updated December 19, 2013. 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.