Establishment registration
DG Instruments
FDA establishment registration 2087382 · GRANTS PASS, US
Key facts
| Registration number | 2087382 |
|---|---|
| Establishment name | DG Instruments |
| Owner/operator | SURGICAL INSTRUMENT |
| Owner/operator number | 9049741 |
| FEI number | 3003697160 |
| Address | 282 LONG ACRES RD |
| City | GRANTS PASS |
| State | OR |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | EGN, EMH, EMI, EML, EMM, FFO, FGN, FHQ, FTY, FZS, FZT, GAD, GDG, GDH, GDJ, GDN, GDZ, GEG, GFF, GFJ, HNF, HRQ, HRR, HSO, HTC, HTD, HTE, HTF, HTJ, HTP and 21 more |
| Device classes | 1 |
At a glance
- 10–99 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