FRANCIS MEDICAL

FDA Device Registration & Listing · Maple Grove, MN, US · Registration 3015975397

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3015975397
FEI Number
3015975397
Entity Name
FRANCIS MEDICAL
City/State/Country
Maple Grove, MN, US
Establishment Address
7351 Kirkwood Ln N, Maple Grove, MN 55369, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Francis Medical (Owner Number: 10095051)
Owner / Operator Contact Address
7351 Kirkwood Lane North, Maple Grove, MN 55369, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K252388
PMA Number
N/A

All Registered Proprietary Names

Vanquish Water Vapor Ablation System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KNS Unit, Electrosurgical, Endoscopic (With Or Without Accessories) Gastroenterology, Urology Class 2 876.4300 2026-01-19

Official Correspondent

Joel Phillips

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Francis Medical
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K172288 Wilson-Cook Medical Inc./Cook Endoscopy Fusion OMNI Sphincterotome 2018-04-17

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015975397. Last updated year: 2026. Please use registration number 3015975397 when referencing this establishment in official correspondence.
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