# Foshan Pingchuang Medical Technology Co., Ltd (manufacturer, Foshan City Guangdong, CN): 4 new FDA device listings, incl. media, coupling, ultrasound

**Score:** 75/100

| Field | Value |
|---|---|
| Establishment | Foshan Pingchuang Medical Technology Co., Ltd |
| Owner / operator | Foshan PingChuang Medical Technology Co., Ltd |
| Role | Manufacturer |
| Establishment types | Manufacture Medical Device |
| Location | Foshan City Guangdong, CN |
| New listings | 4 |
| Devices | Media, Coupling, Ultrasound; Lubricant, Personal; Douche Apparatus, Vaginal, Therapeutic; Enema Kit |
| Product codes | MUI, NUC, HED, FCE |
| Device classes | Class I, Class II |
| Medical specialties | Radiology, Obstetrics/Gynecology, Gastroenterology, Urology |
| Brand names | Non-Sterile Ultrasound Gel Sterile Ultrasound Gel, MOD: 5g,8g,10g,12g,15g,20g,30g,50g,82g,100g,120g,150g,180g,200g; Non-Sterile Ultrasound Gel Sterile Ultrasound Gel, MOD: 250g, 300g, 500g, 1Kg, 1.25L, 1.3L, 2.5L, 5L; CC Lottyplay Hybrid personal lubricant 100ml; Hybrid personal lubricant (water&silicone), MOD: 100ml, 120ml, 150ml, 180ml, 200ml, 250ml, 300ml, 360ml ,500ml; BARWAY Hybrid lubricant Silicone & Water Based 3.38fl.oz.(100ml) x 2PCS; Hybrid personal lubricant(water&silicone), MOD: 5ml, 8ml, 10ml, 12ml, 15ml, 20ml, 30ml, 50ml, 60ml, 75ml, 90ml; Vaginal douche apparatus, Model: 50ml, 80ml, 135ml, 150ml; Enema Kit, Model: 80ml, 120ml, 150ml |
| First new listing | 2026-06-25 |
| Latest new listing | 2026-07-15 |
| FDA registration number | 3014317667 |
| 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.
- 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: 2026-11-04T21:52:36.524Z.
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.