Establishment registration
HISTOTECH ENGINEERING SDN. BHD
FDA establishment registration 3038986585 · Bayan Lepas Pulau Pinang, MY
Key facts
| Registration number | 3038986585 |
|---|---|
| Establishment name | HISTOTECH ENGINEERING SDN. BHD |
| Owner/operator | Histotech Engineering SDN. BHD |
| Owner/operator number | 10096102 |
| FEI number | 3038986585 |
| Address | Plot 46, Hilir Sungai Kluang 2 |
| City | Bayan Lepas Pulau Pinang |
| Country | MY |
| Registration valid through | 2026 |
| Product codes listed | IMS, KNN |
| Device classes | 1 |
At a glance
- 1–9 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