Data / Medical devices / China / Guangdong Maidi Medical Co.,ltd
Guangdong Maidi Medical Co.,ltd: FDA-registered device maker in Qingyuan Guangdong, China, 1 510(k) clearance
Guangdong Maidi Medical Co.,ltd is registered with the FDA (registration 3014627756) in Qingyuan Guangdong, China. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 12, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3014627756
- Address
- No. 3, Zhihui Road, Guangzhou (Qingyuan) industrial Transfer industrialPark Shijiao Town, Qingcheng District, Qingyuan Guangdong, China, 511547
- Owner or operator
- GUANGDONG MAIDI MEDICAL CO.,LTD (10057793)
- Roles
- Manufacturer
- First device listed
- May 27, 2018
- Registered through
- 2026
- Brand names listed
- Face Mask, Packaging Pouch, Self-Seal Sterilization Pouch and Roll
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Face Mask Within The Scope Of The Face Mask And Barrier Face Covering Enforcement Policy Or Face Mask Umbrella Eua | QKR | N | Manufacturer | accessdata.fda.gov |
| Indicator, Physical/Chemical Sterilization Process | JOJ | 2 | Manufacturer | accessdata.fda.gov |
| Instrument, Manual, Surgical, General Use | MDM | 1 | Manufacturer | accessdata.fda.gov |
| Wrap, Sterilization | FRG | 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 |
|---|---|---|---|---|---|---|
| December 12, 2025 | K251177 | Self-Seal Sterilization Pouch and Roll | FRG | Substantially Equivalent | Guangdong Maidi Medical Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Face Mask Within The Scope Of The Face Mask And Barrier Face Covering Enforcement Policy Or Face Mask Umbrella Eua
- All makers of Instrument, Manual, Surgical, General Use
- All makers of Indicator, Physical/Chemical Sterilization Process
- All makers of Wrap, Sterilization
Updated December 12, 2025. 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.