Data / Medical devices / China / Nature Health Development(hong Kong)co.,limited
Nature Health Development(hong Kong)co.,limited: FDA-registered device maker in Hong Kong, China, 3 510(k) clearances
Nature Health Development(hong Kong)co.,limited is registered with the FDA (registration 3035744034) in Hong Kong, China. It lists 2 device types. The FDA files 3 510(k) clearances under its listings, the newest dated June 18, 2025. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3035744034
- Address
- Flat/Rm C6a 15/F TML Tower 3 Hoi Shing Road Tsuen Wan, Hong Kong, China, 999077
- Owner or operator
- WINNER MEDICAL CO., LTD. (9012349)
- Roles
- Exporter to the US
- First device listed
- May 7, 2010
- Registered through
- 2026
- Brand names listed
- Conforming stretch gauze, DRYNET, Earloops Face Mask, Face Mask, LARGE STERILE GAUZE PAD, Medical Earloop Face Mask, Medical Face Mask, Medical Face Mask Earloop and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Gauze / Sponge,Nonresorbable For External Use | NAB | 1 | Exporter to the US | accessdata.fda.gov |
| Mask, Surgical | FXX | 2 | Exporter to the US | 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 18, 2025 | K250082 | Procedure mask/Surgical mask/Face mask | FXX | Substantially Equivalent | Winner Medical Co., Ltd. | accessdata.fda.gov |
| March 6, 2023 | K223232 | Procedure mask/Surgical mask/Face mask | FXX | Substantially Equivalent | Winner Medical Co., Ltd. | accessdata.fda.gov |
| May 17, 2022 | K220194 | Procedure mask/Surgical mask/Face mask | FXX | Substantially Equivalent | Winner Medical Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated June 18, 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.