Establishment registration
CTK BIOTECH, INC.
FDA establishment registration 2032682 · Poway, US
Key facts
| Registration number | 2032682 |
|---|---|
| Establishment name | CTK BIOTECH, INC. |
| Owner/operator | CTK BIOTECH, INC. |
| Owner/operator number | 9051784 |
| FEI number | 3003952975 |
| Address | 13855 Stowe Dr |
| City | Poway |
| State | CA |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | CDD, CDP, CDZ, CEP, CFT, CGJ, CHP, DBF, DCN, DHA, DHR, GND, GNW, GOA, GOM, GPW, GQG, GQI, GQO, GRL, GRT, GRX, GSQ, GTZ, JHI, JIP, JJX, JLB, JLS, JLW and 32 more |
| Device classes | 1, 2, 3, N |
At a glance
- 10–99 Device listings
- None UDI devices (GUDID)
- Current Registration current
- 1–9 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