Data / Medical devices / United States / L C Industries
L C Industries: FDA-registered device maker in Durham, NC, United States, 1 510(k) clearance
L C Industries is registered with the FDA (registration 3003206812) in Durham, NC, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 14, 2018. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3003206812
- Address
- 4500 emperor blvd, Durham, NC, United States, 27703
- Owner or operator
- L C Industries (10059073)
- Roles
- Manufacturer, Repackager or relabeler
- First device listed
- August 18, 2021
- Registered through
- 2026
- Brand names listed
- No Proprietary Name...Made for Military
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| First Aid Kit With Drug | LRR | N | Manufacturer | accessdata.fda.gov |
| Ureteroscope And Accessories, Flexible/Rigid | FGB | 2 | Repackager or relabeler | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| August 14, 2018 | K181977 | WiScope Digital Endoscope System | FGB | Substantially Equivalent | OTU Medical, Inc. | accessdata.fda.gov |
Compare with other makers
Updated August 14, 2018. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.