# Shenzhen Sany Pioneer Technology Co., Ltd. (manufacturer, Shenzhen Guangdong, CN): 5 new FDA device listings, incl. set, tubing and support, ventilator (w harness)

**Score:** 75/100

| Field | Value |
|---|---|
| Establishment | Shenzhen Sany Pioneer Technology Co., Ltd. |
| Owner / operator | Shenzhen Sany Pioneer Technology Co.,Ltd |
| Role | Manufacturer |
| Establishment types | Manufacture Medical Device |
| Location | Shenzhen Guangdong, CN |
| New listings | 5 |
| Devices | Set, Tubing And Support, Ventilator (W Harness); Dilator, Nasal; Device, Anti-Snoring; Device, Jaw Repositioning; Ventilator, Non-Continuous (Respirator) |
| Product codes | BZO, LWF, LRK, LQZ, BZD |
| Device classes | Class I, Class II |
| Medical specialties | Anesthesiology, Ear, Nose, Throat, Dental |
| Brand names | Replacement Short Tube for N20 Series, Integrated CPAP Elbow & Hose; Replacement Tubing and Support Set for P10; Nasal Strips for Snoring (BK01, BK02, B0); Nasal Dilator (BK01, BK02, BK0); Joybloom Anti Snoring Mouthpiece L09; Willnice Anti Snoring Mouthpiece L09; Innoflow Anti Snoring Mouthpiece L09; Cushion |
| First new listing | 2026-05-07 |
| Latest new listing | 2026-09-01 |
| FDA registration number | 3016674860 |
| Registration expires | 2027-12-31 |

## Why this score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.

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: 2026-10-28T20:51:27.468Z.
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.