Establishment registration
Qingdao Leckie Foam Products Co. Ltd.
FDA establishment registration 3007483335 · Qingdao Shandong, CN
Key facts
| Registration number | 3007483335 |
|---|---|
| Establishment name | Qingdao Leckie Foam Products Co. Ltd. |
| Owner/operator | Leckie Medical Products, Inc. |
| Owner/operator number | 10023739 |
| FEI number | 3007483335 |
| Address | Rm. 101, No.2, Building 8 Fen He Road |
| City | Qingdao Shandong |
| Country | CN |
| Establishment types | Manufacturer |
| Registration valid through | 2026 |
| Product codes listed | CBH |
| 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