Establishment registration
ADLER INSTRUMENT COMPANY
FDA establishment registration 3007507973 · Brooksville, US
Key facts
| Registration number | 3007507973 |
|---|---|
| Establishment name | ADLER INSTRUMENT COMPANY |
| Owner/operator | Adler Instruments |
| Owner/operator number | 10028510 |
| FEI number | 3010034765 |
| Address | 16460 Cortez Blvd |
| City | Brooksville |
| State | FL |
| Country | US |
| Establishment types | Single-use device reprocessor |
| Registration valid through | 2026 |
| Product codes listed | DWP, DWS, EIG, EKT, EMG, EMJ, EPY, FFN, FGN, FHQ, FTY, FZO, GAC, GAD, GDG, GDI, GDJ, GDN, GDR, GDZ, GEA, GEG, GEN, GFI, GFJ, GTZ, GZT, GZX, HAO, HCY and 51 more |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- 100–999 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