Establishment registration
Lincotek Medical LLC
FDA establishment registration 3010039400 · Vandalia, US
Key facts
| Registration number | 3010039400 |
|---|---|
| Establishment name | Lincotek Medical LLC |
| Owner/operator | Lincotek Medical, LLC |
| Owner/operator number | 9057128 |
| FEI number | 3010039400 |
| Address | 811 Northwoods Blvd |
| City | Vandalia |
| State | OH |
| Country | US |
| Establishment types | Export-only manufacturer |
| Registration valid through | 2026 |
| Product codes listed | FZX, GAB, GXZ, HRS, HRY, HSD, HSN, HSX, HTJ, HTQ, HWA, HWB, HWC, HWE, HWT, HXG, HXK, JDI, JDN, JWH, KRO, KRR, KWS, KWT, KWZ, LPH, LWJ, LXH, LZO, MAX and 6 more |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- 100–999 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