510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K153568Substantially Equivalent

InMode Plus System

Inmode MD, Ltd., Yokneam, IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K153568 is the FDA 510(k) clearance record for InMode Plus System, a class II device, cleared for Inmode MD , Ltd. on under FDA product code PBX (Massager, Vacuum, Radio Frequency Induced Heat). FDA's definition for product code PBX reads: "Generates heat in body tissues for minor relief of minor aches and pain. Mechanical massaging to provide a temporary reduction in the appearance of cellulite". FDA records list 21 510(k) clearances for Inmode MD , Ltd., from to . As of , FDA records show no recalls naming K153568.

Clearance record

Decision date
Received
(211 days to decision)
Product code
PBX Massager, Vacuum, Radio Frequency Induced Heat
Regulation
21 CFR 878.4400
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Inmode MD , Ltd. Tabor Bldg., Shaar Yokneam, Yokneam, IL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code PBX

Trailing 12 months
5 clearances under product code PBX in the twelve months to October 2026, March 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code PBX, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20262
April 20261
May 20260
June 20260
July 20261
August 20260
September 20261
October 20260