# Guangzhou Decheng Biotechnology Co., Ltd. (manufacturer, Guangzhou Guangdong, CN): 2 new FDA device listings, incl. kit, test, pregnancy, hcg, over the counter

**Score:** 70/100

| Field | Value |
|---|---|
| Establishment | Guangzhou Decheng Biotechnology Co., Ltd. |
| Owner / operator | Guangzhou Decheng biotechnology co., Ltd. |
| Role | Manufacturer |
| Establishment types | Manufacture Medical Device |
| Location | Guangzhou Guangdong, CN |
| New listings | 2 |
| Devices | Kit, Test, Pregnancy, Hcg, Over The Counter; Radioimmunoassay, Estrone |
| Product codes | LCX, CGF |
| Device classes | Class I, Class II |
| Medical specialties | Clinical Chemistry |
| Brand names | easy@Home® Digital Pregnancy Test; premom® E3G Quantitative Test |
| First new listing | 2026-09-27 |
| Latest new listing | 2026-09-28 |
| FDA registration number | 3017904598 |
| Registration expires | 2026-12-31 |

## Why this score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Class II or III devices: QMS and regulatory demands.
- Listed in the last 45 days.

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.