510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K922473Substantially Equivalent

Turn Ez Bed Device

Med-Ez, Inc., Reidsville NC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K922473 is the FDA 510(k) clearance record for TURN EZ BED DEVICE, a class II device, cleared for Med-Ez, Inc. on under FDA product code IKZ (Bed, Patient Rotation, Powered). FDA records list one 510(k) clearance for Med-Ez, Inc. As of , FDA records show no recalls naming K922473.

Clearance record

Decision date
Received
(106 days to decision)
Product code
IKZ Bed, Patient Rotation, Powered
Regulation
21 CFR 890.5225
Device class
Class II
Review panel
Physical Medicine
Applicant
Med-Ez, Inc. 2400 Gibbs Dr., Reidsville NC
510(k) summary
Statement
Third party review
No

Clearances, product code IKZ

Trailing 12 months

FDA records hold no clearances under product code IKZ in the trailing twelve months.

FDA records show no clearances under product code IKZ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code IKZ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260