Establishment registration
SUZHOU ENDOPHIX CO., LTD.
FDA establishment registration 3030514683 · Suzhou Jiangsu, CN
Key facts
| Registration number | 3030514683 |
|---|---|
| Establishment name | SUZHOU ENDOPHIX CO., LTD. |
| Owner/operator | Suzhou Endophix Co., Ltd. |
| Owner/operator number | 10089613 |
| FEI number | 3030514683 |
| Address | Room 202, Factory No.3, Lane 151, Fengli Road, SIP, 215000 Suzhou, Jiangsu Province, P.R. CHINA |
| City | Suzhou Jiangsu |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | FZX, GFA, HTD, HTJ, HTN, HTP, HTS, HTW, HWC, HWJ, HXB, HXI, HXX, KIL, LXH, MBI, NBH |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- 100–999 UDI devices (GUDID)
- Current Registration current
- None FDA inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device establishment registrations
Device establishments that manufacture, repackage, relabel or import devices for the U.S. market must register annually with the FDA and list the devices they produce.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database