Data / Medical devices / United States / Wep, LLC
Wep, LLC: FDA-registered device maker in Wrightsville, GA, United States, 1 510(k) clearance
Wep, LLC is registered with the FDA (registration 3005615323) in Wrightsville, GA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated April 11, 1994. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3005615323
- Address
- 2390 Idylwild Dr, Wrightsville, GA, United States, 31096
- Owner or operator
- WEP, LLC (10040298)
- Roles
- Repackager or relabeler
- First device listed
- March 29, 2012
- Registered through
- 2026
- Brand names listed
- Sawhorse, Sawhorse Brand
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Sunglasses (Non-Prescription Including Photosensitive) | HQY | 1 | 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 |
|---|---|---|---|---|---|---|
| April 11, 1994 | K940944 | DAY SUN INDUSTRIAL CORP | HQY | Substantially Equivalent | Day Sun Industrial Corp. | accessdata.fda.gov |
Compare with other makers
Updated April 11, 1994. 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.