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

Legend X Platform

K Number: K252576 · Decision Sep 12, 2025
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
18
Review Days
29

Basic Information

Device Name
Legend X Platform
K Number
K252576
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Pollogen, Ltd.
Date Received
August 14, 2025
Decision Date
September 12, 2025
Product Code
GEI
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
NE
Third Party
Y

Classifications

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

Product Code Device Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

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K Number Device Name
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K232903 Legend X Platform
K220322 Pollogen STOP U Model UXV Device
K220124 YandR System, VoluDerm Handpiece, VoluDerm Tips
K200545 Legend Pro DMA
K203665 STOP U Model UXV Device
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