Establishment registration
ACUMED INSTRUMENTS CORP.
FDA establishment registration 2083124 · Santa Barbara, US
Key facts
| Registration number | 2083124 |
|---|---|
| Establishment name | ACUMED INSTRUMENTS CORP. |
| Owner/operator | ACUMED INSTRUMENTS CORP. |
| Owner/operator number | 2083124 |
| FEI number | 2083124 |
| Address | 1050 Vista de la Mesa Drive |
| City | Santa Barbara |
| State | CA |
| Country | US |
| Establishment types | Specification developer |
| Registration valid through | 2026 |
| Product codes listed | EQJ |
| Device classes | 1 |
At a glance
- 1–9 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