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13 devices found
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sorted by relevance
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Manufacturer: Francis Medical, Inc.
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Device · Manufacturer · Authorizations
Verified
Status
Regime
Registry
Class
Vanquish Water Vapor Ablation System 4570-001
Francis Medical, Inc.
·
,
FDA registration: United States
Class II
GUDID
on market
None
GUDID
II
Vanquish Water Vapor Ablation System 4571-001
Francis Medical, Inc.
·
,
FDA registration: United States
Class II
GUDID
on market
None
GUDID
II
Vanquish Water Vapor Ablation System 4572-001
Francis Medical, Inc.
·
,
FDA registration: United States
Class II
GUDID
on market
None
GUDID
II
Vanquish Water Vapor Ablation System 4573-001
Francis Medical, Inc.
·
,
FDA registration: United States
Class II
GUDID
on market
None
GUDID
II
Vanquish Water Vapor Ablation System 5245-001
Francis Medical, Inc.
·
,
FDA registration: United States
Class II
GUDID
on market
None
GUDID
II
Vanquish Water Vapor Ablation System 5257-001
Francis Medical, Inc.
·
,
FDA registration: United States
Class II
GUDID
on market
None
GUDID
II
Vanquish Water Vapor Ablation System 4751-001
Francis Medical, Inc.
·
,
FDA registration: United States
Class II
GUDID
on market
None
GUDID
II
Vanquish Water Vapor Ablation System 4752-001
Francis Medical, Inc.
·
,
FDA registration: United States
Class II
GUDID
on market
None
GUDID
II
Vanquish Water Vapor Ablation System 4741-001
Francis Medical, Inc.
·
,
FDA registration: United States
Class II
GUDID
on market
None
GUDID
II
Vanquish Water Vapor Ablation System 4839-001
Francis Medical, Inc.
·
,
FDA registration: United States
Class II
GUDID
on market
None
GUDID
II
Vanquish Water Vapor Ablation System 4840-001
Francis Medical, Inc.
·
,
FDA registration: United States
Class II
GUDID
on market
None
GUDID
II
Vanquish Water Vapor Ablation System 5536-001
Francis Medical, Inc.
·
,
FDA registration: United States
Class II
GUDID
on market
None
GUDID
II
Vanquish Water Vapor Ablation Device
Francis Medical, Inc.
·
,
FDA registration: United States
Class II
FDA 510(k)
K252388
Active
Cleared 26 Nov 2025
Active
510(k)
510(k)
II
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