510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K241822Substantially Equivalent

ReWalk® 7 Personal Exoskeleton (50-20-0005)

Rewalk Robotics Ltd. dba Lifeward, Yokneam Ilit, IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K241822 is the FDA 510(k) clearance record for ReWalk® 7 Personal Exoskeleton (50-20-0005), a class II device, cleared for Rewalk Robotics Ltd. Dba Lifeward on under FDA product code PHL (Powered Exoskeleton). FDA's definition for product code PHL reads: "A powered exoskeleton is a prescription device that is composed of an external, powered, motorized orthosis that is placed over a person's paralyzed or weakened lower extremity limb(s) for medical purposes". FDA records list one 510(k) clearance for Rewalk Robotics Ltd. Dba Lifeward. As of , FDA records show no recalls naming K241822.

Clearance record

Decision date
Received
(261 days to decision)
Product code
PHL Powered Exoskeleton
Regulation
21 CFR 890.3480
Device class
Class II
Review panel
Physical Medicine
Applicant
Rewalk Robotics Ltd. Dba Lifeward 3 Hatnufa St., P.O Box 161, Yokneam Ilit, IL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code PHL

Trailing 12 months
2 clearances under product code PHL in the twelve months to October 2026, August 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code PHL, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20261
September 20261
October 20260