Data / Medical devices / United States / Aso LLC
Aso LLC: FDA-registered device maker in Palmetto, FL, United States, 1 510(k) clearance
Aso LLC is registered with the FDA (registration 3025145822) in Palmetto, FL, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated February 17, 1999. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3025145822
- Address
- 2330 S Dock Street, Palmetto, FL, United States, 34221
- Owner or operator
- ASO LLC (1038758)
- Roles
- Repackager or relabeler
- First device listed
- January 12, 2004
- Registered through
- 2027
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Tape And Bandage, Adhesive | KGX | 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 |
|---|---|---|---|---|---|---|
| February 17, 1999 | K983368 | CARE BAND ANTIBACTERIAL BANDAGES | KGX | Substantially Equivalent | Aso Corp. | accessdata.fda.gov |
Compare with other makers
Updated February 17, 1999. 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.