Establishment registration
HORIBA INSTRUMENTS INCORPORATED
FDA establishment registration 1827821 · Canton, US
Key facts
| Registration number | 1827821 |
|---|---|
| Establishment name | HORIBA INSTRUMENTS INCORPORATED |
| Owner/operator | HORIBA INSTRUMENTS INCORPORATED (DBA) HORIBA Medical |
| Owner/operator number | 10083022 |
| FEI number | 1827821 |
| Address | 5449 Research Dr |
| City | Canton |
| State | MI |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | CDL, CDP, CDQ, CDT, CDZ, CEC, CEK, CEM, CEO, CEP, CFJ, CFR, CFT, CGA, CGJ, CGS, CGX, CGZ, CHA, CHH, CHI, CHP, CIC, CIG, CIJ, CIT, CIX, CJE, CKA, DBF and 68 more |
| Device classes | 1, 2, U |
At a glance
- 100–999 Device listings
- 1,000+ 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