Establishment registration
SPLINT FACTORY CORP.
FDA establishment registration 3045954439 · Port Townsend, US
Key facts
| Registration number | 3045954439 |
|---|---|
| Establishment name | SPLINT FACTORY CORP. |
| Owner/operator | Splint Factory Corp. |
| Owner/operator number | 10095940 |
| FEI number | 3045954439 |
| Address | 2330 Rosecrans St |
| City | Port Townsend |
| State | WA |
| Country | US |
| Establishment types | Manufacturer, Specification developer |
| Registration valid through | 2026 |
| Product codes listed | ILH |
| 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