Data / Medical devices / Hong Kong / Hong Kong Lanli Technology Co., Limited
Hong Kong Lanli Technology Co., Limited: FDA-registered device maker in Tuen Mun, Hong Kong, 2 510(k) clearances
Hong Kong Lanli Technology Co., Limited is registered with the FDA (registration 3034397208) in Tuen Mun, Hong Kong. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated May 15, 2015. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3034397208
- Address
- Shop 185 G/F, Hang Wai Ind. Centre, No.6 Kin Tai ST., Tuen Mun, Hong Kong, 999077
- Owner or operator
- Hong Kong Lanli Technology Co., Limited (10092134)
- Roles
- Foreign private label distributor, Remanufacturer, Repackager or relabeler
- First device listed
- May 19, 2026
- Registered through
- 2026
- Brand names listed
- Personal Steam Inhaler, Vocal Steamer for Sinus Relief, Allergies, Congestion & Colds, Propeller System - Compressor Nebulizer for Adults and Kids,Personal Cool Mist Jet Nebulizer Machine for Breathing Home
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Humidifier, Non-Direct Patient Interface (Home-Use) | KFZ | 1 | Foreign private label distributor, Repackager or relabeler | accessdata.fda.gov |
| Nebulizer (Direct Patient Interface) | CAF | 2 | Remanufacturer, Repackager or relabeler | 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 15, 2015 | K142516 | Propeller System | CAF | Substantially Equivalent | Reciprocal Labs Corporation | accessdata.fda.gov |
| February 10, 1995 | K950116 | THERASTEAM PERSONAL STEAM INHALER | KFZ | Substantially Equivalent | Kaz, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Humidifier, Non-Direct Patient Interface (Home-Use)
- All makers of Nebulizer (Direct Patient Interface)
Updated May 15, 2015. 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.