Data / Medical devices / United States / Best Sanitizers, Inc.
Best Sanitizers, Inc.: FDA-registered device maker in Walton, KY, United States, 1 510(k) clearance
Best Sanitizers, Inc. is registered with the FDA (registration 3005763425) in Walton, KY, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated February 5, 2010. 1 recall event names it as the recalling firm. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3005763425
- Address
- 154 Mullen Dr, Walton, KY, United States, 41094
- Owner or operator
- Best Sanitizers (9065257)
- Roles
- Manufacturer
- First device listed
- March 16, 2011
- Registered through
- 2026
- Brand names listed
- Acecide-C
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Sterilant, Medical Devices | MED | 2 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| February 5, 2010 | K091210 | ACECIDE-C HIGH LEVEL DISINFECTANT AND STERILANT | MED | Substantially Equivalent | Best Sanitizers, Inc. | accessdata.fda.gov |
Recalls
Recall events where this establishment is the recalling firm, matched on its FEI.
| Initiated | Event | Class | Status | Product | Reason | Source |
|---|---|---|---|---|---|---|
| August 2, 2016 | 74862 | Class II | Terminated | Acecide-C High Level Disinfectant & Sterilant 875 mL. Packaging is 6 inner cartons in one master carton;1 inner carton consists of a set of two liquids (1 acid & 1 buffer) banded together. | Certain lots of the acid solution in Acecide-C are degrading faster than normal. | accessdata.fda.gov |
Compare with other makers
Updated September 2, 2016. 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.