# Suzhou Zenith Vascular Scitech Limited (manufacturer, Suzhou Jiangsu, CN): 7 new FDA device listings, incl. catheter, percutaneous

**Score:** 75/100

| Field | Value |
|---|---|
| Establishment | Suzhou Zenith Vascular Scitech Limited |
| Owner / operator | Suzhou Zenith Vascular SciTech Limited |
| Role | Manufacturer |
| Establishment types | Manufacture Medical Device |
| Location | Suzhou Jiangsu, CN |
| New listings | 7 |
| Devices | Catheter, Percutaneous; Catheter, Percutaneous, Neurovasculature; Catheter, Thrombus Retriever; Catheter, Continuous Flush; Guide, Wire, Catheter, Neurovasculature; Wire, Guide, Catheter |
| Product codes | DQY, QJP, NRY, KRA, MOF, DQX |
| Device classes | Class II |
| Medical specialties | Cardiovascular |
| Brand names | Zenith Distal Access Long Sheath; Zenith Aspiration Catheter; Disposable Aspiration Tubing Set; Micro Catheter; Zenith Micro Guidewire |
| First new listing | 2026-05-21 |
| Latest new listing | 2026-06-07 |
| FDA registration number | 3039020025 |
| 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.