Data / Medical devices / China / Shenzhen Kingboom Technology Co., Ltd
Shenzhen Kingboom Technology Co., Ltd: FDA-registered device maker in Shenzhen Guangdong, China, 3 510(k) clearances
Shenzhen Kingboom Technology Co., Ltd is registered with the FDA (registration 3038634684) in Shenzhen Guangdong, China. It lists 1 device type. The FDA files 3 510(k) clearances under its listings, the newest dated May 12, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3038634684
- Address
- #201,2nd fl,No.5,Tongxin Road,Pingdong Community,Pingdi Street,Longgang District, Shenzhen Guangdong, China, 518000
- Owner or operator
- Shenzhen Kingboom Technology Co., Ltd (10093560)
- Roles
- Manufacturer
- First device listed
- June 3, 2025
- Registered through
- 2026
- Brand names listed
- Electric Nasal Aspirator BC027,BC030,BC033,BC035,BC035B, Electric nasal aspirator BCO26, BCO25, BC023, BC028, BC029, BCO36, Nasal Aspirator model BC023.BC025.BC026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Pump, Portable, Aspiration (Manual Or Powered) | BTA | 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 |
|---|---|---|---|---|---|---|
| May 12, 2026 | K260473 | Electric nasal aspirator (BC027, BC030, BC033, BC035, BC035B) | BTA | Substantially Equivalent | Shenzhen Kingboom Technology Co., Ltd. | accessdata.fda.gov |
| March 13, 2026 | K260147 | Electric nasal aspirator (BC026, BC025, BC023, BC028, BC029, BC036) | BTA | Substantially Equivalent | Shenzhen Kingboom Technology Co., Ltd. | accessdata.fda.gov |
| April 23, 2025 | K250697 | Electric Nasal Aspirator (BC026, BC025, BC023) | BTA | Substantially Equivalent | Shenzhen Kingboom Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated May 12, 2026. 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.