Data / Medical devices / United States / Kenco Logistic Services, LLC
Kenco Logistic Services, LLC: FDA-registered device maker in Chattanooga, TN, United States, 9 510(k) clearances
Kenco Logistic Services, LLC is registered with the FDA (registration 3004895419) in Chattanooga, TN, United States. It lists 21 device types. The FDA files 9 510(k) clearances under its listings, the newest dated March 24, 2017. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3004895419
- Address
- 4309 Distribution Dr, Chattanooga, TN, United States, 37416
- Owner or operator
- Kenco Logistics Services, LLC (10056810)
- Roles
- Repackager or relabeler
- First device listed
- April 28, 2026
- Registered through
- 2027
Devices it lists
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 |
|---|---|---|---|---|---|---|
| March 24, 2017 | K162342 | Stellaris Elite Vision Enhancement System | HQC | Substantially Equivalent | Bausch+Lomb | accessdata.fda.gov |
| September 11, 2015 | K151604 | 23ga Chandelier Illuminator, 25ga Chandelier Illuminator | MPA | Substantially Equivalent | Peregrine Surgical , Ltd. | accessdata.fda.gov |
| January 9, 2014 | K131958 | BAUSCH & LOMB INJECTOR SYSTEM | MSS | Substantially Equivalent | Bausch & Lomb | accessdata.fda.gov |
| September 28, 2012 | K113852 | BAUSCH & LOMB IOL INJECTOR | MSS | Substantially Equivalent | Bausch & Lomb, Inc. | accessdata.fda.gov |
| March 12, 2008 | K073023 | STERILS SINGLE-USE I/A HANDPIECES | HQC | Substantially Equivalent | Bausch & Lomb, Inc. | accessdata.fda.gov |
| March 7, 2007 | K063694 | AKREOS SINGLE USE INSERTION DEVICE, MODEL AI-28 | KYB | Substantially Equivalent | Bausch & Lomb, Inc. | accessdata.fda.gov |
| December 19, 2006 | K063331 | BAUSCH & LOMB NGX MICROSURGICAL SYSTEM | HQC | Substantially Equivalent | Bausch & Lomb, Inc. | accessdata.fda.gov |
| September 1, 1995 | K952586 | GAMP & ASSOCIATES DISPOSABLE FIBEROPTIC ENDOILLUMINATOR | MPA | Substantially Equivalent | Gamp & Assoc. | accessdata.fda.gov |
| August 17, 1988 | K882802 | STORZ DISPOSABLE BIPOLAR PENCILS | GXI | Substantially Equivalent | Storz Instrument Co. | accessdata.fda.gov |
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Updated March 24, 2017. 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.