Data / Medical devices / United States / Francis Medical
Francis Medical: FDA-registered device maker in Maple Grove, MN, United States, 1 510(k) clearance
Francis Medical is registered with the FDA (registration 3015975397) in Maple Grove, MN, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 26, 2025. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3015975397
- Address
- 7351 Kirkwood Ln N, Maple Grove, MN, United States, 55369
- Owner or operator
- Francis Medical (10095051)
- Roles
- Manufacturer
- First device listed
- January 19, 2026
- Registered through
- 2027
- Brand names listed
- Vanquish Water Vapor Ablation System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Unit, Electrosurgical, Endoscopic (With Or Without Accessories) | KNS | 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 |
|---|---|---|---|---|---|---|
| November 26, 2025 | K252388 | Vanquish Water Vapor Ablation Device | KNS | Substantially Equivalent | Francis Medical, Inc. | accessdata.fda.gov |
Compare with other makers
Updated November 26, 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.