Data / Medical devices / United States / Kenco Logistic Services, LLC
Kenco Logistic Services, LLC: FDA-registered device maker in Perris, CA, United States, 2 510(k) clearances
Kenco Logistic Services, LLC is registered with the FDA (registration 3017195494) in Perris, CA, United States. It lists 5 device types. The FDA files 2 510(k) clearances under its listings, the newest dated June 20, 2013. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3017195494
- Address
- 4120 Indian Ave Ste 150, Perris, CA, United States, 92571
- Owner or operator
- Kenco Logistics Services, LLC (10056810)
- Roles
- Repackager or relabeler
- First device listed
- January 19, 2018
- Registered through
- 2027
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Tampon, Menstrual, Scented, Scented-Deodorized | HIL | 2 | Repackager or relabeler | accessdata.fda.gov |
| Floss, Dental | JES | 1 | Repackager or relabeler | accessdata.fda.gov |
| Tampon, Menstrual, Unscented | HEB | 2 | Repackager or relabeler | accessdata.fda.gov |
| Toothbrush, Manual | EFW | 1 | Repackager or relabeler | accessdata.fda.gov |
| Toothbrush, Powered | JEQ | 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 |
|---|---|---|---|---|---|---|
| June 20, 2013 | K131543 | TAMPAX(R) L PLASTIC TAMPONS, UNSCENTED | HEB | Substantially Equivalent | Procter & Gamble Co. | accessdata.fda.gov |
| June 21, 2012 | K120245 | PLAYTEX GENTLE GLIDE SCENTED TAMPONS AND PLAYTEX GENTLE GLIDE UNSCENTED TAMPONS | HIL | Substantially Equivalent | Playtex, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Toothbrush, Manual
- All makers of Toothbrush, Powered
- All makers of Tampon, Menstrual, Unscented
- All makers of Floss, Dental
- All makers of Tampon, Menstrual, Scented, Scented-Deodorized
Updated June 20, 2013. 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.