Data / Medical devices / United States / KA Medical
KA Medical: FDA-registered device maker in Arden Hills, MN, United States, 1 510(k) clearance
KA Medical is registered with the FDA (registration 3012276280) in Arden Hills, MN, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated April 17, 2019. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3012276280
- Address
- 1265 Grey Fox Road Suite 550, Arden Hills, MN, United States, 55112
- Owner or operator
- Merit Medical Systems, Inc. (1721504)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- December 14, 2020
- Registered through
- 2027
- Brand names listed
- Micro Plug Set, Siege Vascular Plug
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Vascular, For Promoting Embolization | KRD | 2 | Contract manufacturer, 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 |
|---|---|---|---|---|---|---|
| April 17, 2019 | K182944 | Dr. Amplatz Micro Plug | KRD | Substantially Equivalent | Ka Medical, LLC | accessdata.fda.gov |
Compare with other makers
Updated April 17, 2019. 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.