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

Sensilift Pro (ST300XXYYZZZ)

K Number: K250341 · Decision Jan 6, 2026
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
11
Applicant Total
12
Review Days
334

Basic Information

Device Name
Sensilift Pro (ST300XXYYZZZ)
K Number
K250341
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4420
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
El Global Trade, Ltd.
Date Received
February 6, 2025
Decision Date
January 6, 2026
Product Code
PAY
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
PAY Over-The-Counter Radiofrequency Coagulation Device For Wrinkle Reduction

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (PAY), ordered by most recent decision date.

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Other Clearances by El Global Trade, Ltd.

K Number Device Name
K252621 DeepSkin (DEP100)
K250384 IPL400
K232424 CurrentBody Skin RF
K183260 Sensilight Pro / Pistol IPL
K181095 RF-Relief
K172181 micro IPL
K170637 sensiFirm
K170499 sensiLift
K161089 sensiLight Mini
K140381 SENSILIGHT/ SENSILIGHT PLUS
Search all 12 clearances from El Global Trade, Ltd. →