Establishment registration
HOYA Corporation PENTAX Lifecare Division
FDA establishment registration 3003782610 · KURIHARA-SHI Miyagi, JP
Key facts
| Registration number | 3003782610 |
|---|---|
| Establishment name | HOYA Corporation PENTAX Lifecare Division |
| Owner/operator | HOYA Corporation PENTAX Division |
| Owner/operator number | 8030235 |
| FEI number | 3003782610 |
| Address | 30-2 Okada, Aza-Shimomiyano, Tsukidate |
| City | KURIHARA-SHI Miyagi |
| Country | JP |
| Registration valid through | 2026 |
| Product codes listed | CAL, EOB, EOQ, EOX, EQL, FAJ, FAM, FBN, FCW, FCY, FDF, FDI, FDS, FDT, FEA, FEM, FET, FGB, GCL, GEI, ITX, KGE, MNK, MNL, OCX, ODC, ODG, OUG, PEA |
| Device classes | 1, 2 |
At a glance
- 10–99 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