FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

XSense Cryoablation System with CryoProbes

K Number: K260377 · Decision Feb 24, 2026
Classifications
1
FEI Numbers
83
Registration Numbers
83
Same Product Code
261
Applicant Total
4
Review Days
19

Basic Information

Device Name
XSense Cryoablation System with CryoProbes
K Number
K260377
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.4350
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
IceCure Medical , Ltd.
Date Received
February 5, 2026
Decision Date
February 24, 2026
Product Code
GEH
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GEH Unit, Cryosurgical, Accessories

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Other Clearances by IceCure Medical , Ltd.

K Number Device Name
K240892 XSense Cryoablation System with Cryoprobes
K183213 IceSense 3, ProSense, MultiSense
K102360 ICESENCE 3