Establishment registration
SHENZHEN SPONGE NEW MATERIAL CO. LTD
FDA establishment registration 3043106338 · Shenzhen Guangdong, CN
Key facts
| Registration number | 3043106338 |
|---|---|
| Establishment name | SHENZHEN SPONGE NEW MATERIAL CO. LTD |
| Owner/operator | Shenzhen Sponge New Material Co. LTD |
| Owner/operator number | 10094571 |
| FEI number | 3043106338 |
| Address | Pingshan Linhui Road,21 Zhongcheng Medical Industry Park,Block A,6/F |
| City | Shenzhen Guangdong |
| Country | CN |
| Establishment types | Manufacturer |
| Registration valid through | 2026 |
| Product codes listed | NAB |
| Device classes | 1 |
At a glance
- 1–9 Device listings
- None 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