Data / Medical devices / China / Qingdao Future Medical Technology Co., Ltd.
Qingdao Future Medical Technology Co., Ltd.: FDA-registered device maker in Qingdao Shandong, China, 2 510(k) clearances
Qingdao Future Medical Technology Co., Ltd. is registered with the FDA (registration 3014866140) in Qingdao Shandong, China. It lists 4 device types. The FDA files 2 510(k) clearances under its listings, the newest dated November 14, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3014866140
- Address
- SouthB1 Building E,No.621 Jiushui Rd,Laoshan District, Qingdao Shandong, China, 266000
- Owner or operator
- Qingdao Future Medical Technology Co., Ltd. (10058479)
- Roles
- Manufacturer
- First device listed
- October 4, 2018
- Registered through
- 2026
- Brand names listed
- Adlut Mask (H6), Child Mask (H6), Intelligent Mesh Nebulizer (NEB001), Intelligent Mesh Nebulizer (NEB002), Mesh Nebulizer (H6), Mouthpiece (H6), Nebulizer Accessory Set (H6HC), Nebulizer Cup (H6)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Mask, Oxygen | BYG | 1 | Manufacturer | accessdata.fda.gov |
| Mouthpiece, Breathing | BYP | 1 | Manufacturer | accessdata.fda.gov |
| Nebulizer (Direct Patient Interface) | CAF | 2 | Manufacturer | accessdata.fda.gov |
| Nebulizer, Medicinal, Non-Ventilatory (Atomizer) | CCQ | 1 | 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 |
|---|---|---|---|---|---|---|
| November 14, 2025 | K251659 | Mesh Nebulizer (H6) | CAF | Substantially Equivalent | Qingdao Future Medical Technology Co., Ltd. | accessdata.fda.gov |
| August 31, 2018 | K171549 | Intelligent Mesh Nebulizer | CAF | Substantially Equivalent | Qingdao Future Medical Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Mouthpiece, Breathing
- All makers of Mask, Oxygen
- All makers of Nebulizer, Medicinal, Non-Ventilatory (Atomizer)
- All makers of Nebulizer (Direct Patient Interface)
Updated November 14, 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.