510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K905390Substantially Equivalent

Kudo (Powered Rotation Bed)

KCI USA, Inc., San Antonio TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K905390 is the FDA 510(k) clearance record for KUDO (POWERED ROTATION BED), a class II device, cleared for Kinetic Concepts, Inc. on under FDA product code IKZ (Bed, Patient Rotation, Powered). FDA records list 76 510(k) clearances for KCI USA, INC., from to . As of , FDA records show no recalls naming K905390.

Clearance record

Decision date
Received
(39 days to decision)
Product code
IKZ Bed, Patient Rotation, Powered
Regulation
21 CFR 890.5225
Device class
Class II
Review panel
Physical Medicine
Applicant
Kinetic Concepts, Inc. P.O. Box 8588, San Antonio TX
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