Data / Medical devices / Pad, Alcohol, Device Disinfectant / United States
FDA-registered makers of Pad, Alcohol, Device Disinfectant in the United States: 9 establishments
9 establishments in the United States are registered with the FDA to make Pad, Alcohol, Device Disinfectant (product code LKB). 3 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Pad, Alcohol, Device Disinfectant
- Product code
- LKB
- Country
- United States
Makers of Pad, Alcohol, Device Disinfectant in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Becton Dickinson | Franklin Lakes, NJ, United States | Specification developer | 1 | March 20, 2013 | 0 | 0 | 0 | api.fda.gov |
| Professional Disposables International, Inc. | Orangeburg, NY, United States | Manufacturer | 1 | August 27, 2014 | 0 | 0 | 0 | api.fda.gov |
| TNG Worldwide Inc | New Hudson, MI, United States | Specification developer | 1 | March 20, 2013 | 0 | 0 | 0 | api.fda.gov |
| A-1 Creative Packaging LLC | Fort Atkinson, WI, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cardinal Health | Hazelwood, MO, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cardinal Health | Augusta, GA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Frantz Medical Development, Ltd. | Mentor, OH, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Health Line International Corporation | Salt Lake City, UT, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MEDLINE INDUSTRIES, LP - Northfield | Northfield, IL, United States | Specification developer | 0 | 0 | 1 | 0 | api.fda.gov |
Updated November 2, 2026. 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.