Data / Medical devices / United States / Minnesota Medical Technologies
Minnesota Medical Technologies: FDA-registered device maker in Stewartville, MN, United States, 1 510(k) clearance
Minnesota Medical Technologies is registered with the FDA (registration 3015860550) in Stewartville, MN, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated July 22, 2025. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3015860550
- Address
- 2446 Henry Road NW, Stewartville, MN, United States, 55976
- Owner or operator
- Minnesota Medical Technologies (10061310)
- Roles
- Manufacturer
- First device listed
- September 18, 2025
- Registered through
- 2027
- Brand names listed
- My Miracle, Navina, StaySure
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Rectal Insert | PBP | 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 |
|---|---|---|---|---|---|---|
| July 22, 2025 | K243367 | Minnesota Medical Technologies Fecal Incontinence Insert (My Miracle) | PBP | Substantially Equivalent | Minnesota Medical Technologies | accessdata.fda.gov |
Updated July 22, 2025. 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.