Establishment registration
LABOTEK GROUP CORP
FDA establishment registration 3010194621 · Bayamon, US
Key facts
| Registration number | 3010194621 |
|---|---|
| Establishment name | LABOTEK GROUP CORP |
| Owner/operator | LABOTEK GROUP CORP. |
| Owner/operator number | 10044096 |
| FEI number | 3010194621 |
| Address | CARR 174 KM 4.5 BO JUAN SANCHEZ |
| City | Bayamon |
| State | PR |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | DGR, FMK, GAX, GGY, GHC, GHO, GIO, GJG, GJW, GKM, GKQ, GLE, GLG, IDM, IDO, IDZ, IFP, IGG, IQG, JJF, JJG, JKA, JPH, JQW, JRB, JRC, JRI, JRJ, JRO, JRQ and 26 more |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- 100–999 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