# Hong Kong Lanli Technology Co., Limited (repackager or relabeler, Tuen Mun, HK): 2 new FDA device listings, incl. humidifier, non-direct patient interface (home-use)

**Score:** 40/100

| Field | Value |
|---|---|
| Establishment | Hong Kong Lanli Technology Co., Limited |
| Role | Repackager or relabeler |
| Establishment types | Foreign Private Label Distributor; Repack or Relabel Medical Device; Remanufacture Medical Device |
| Location | Tuen Mun, HK |
| New listings | 2 |
| Devices | Humidifier, Non-Direct Patient Interface (Home-Use); Nebulizer (Direct Patient Interface) |
| Product codes | KFZ, CAF |
| Device classes | Class I, Class II |
| Medical specialties | Anesthesiology |
| Brand names | 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 |
| First new listing | 2026-05-19 |
| Latest new listing | 2026-09-11 |
| FDA registration number | 3034397208 |
| Registration expires | 2026-12-31 |

## Why this score
- Class II or III devices: QMS and regulatory demands.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-11-04T21:52:36.524Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.