ClearanceBrief
Company

Arjohuntleigh Magog

FDA 510(k) clearances and medical device recalls filed under this name. Name variants (Inc, Corp, punctuation) are merged.

0510(k) clearances (0 in 12 months)
6recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
FSALift, Patient, Non-Ac-Powered5
IKZBed, Patient Rotation, Powered1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
No clearances in this window.

Latest recalls

DateFirm and productCodeLinked 510(k)
May 24, 2023Arjohuntleigh Magog, Inc.
Arjo Portable Scale Adaptor, Model Number 700.05725; accessory intended to be used in combination with compatible patient lifting equipment
Open, Classified
FSANone listed
Mar 4, 2021Arjohuntleigh Magog, Inc.
Maxi Sky 1000 (Arjo) and V10 (BHM) Bariatric Ceiling Rail - Mounted Lift with measuring function
Terminated
FSANone listed
Oct 6, 2020Arjohuntleigh Magog, Inc.
Arjo Flat Dynamic Positioning System (DPS) - Product Usage: used in conjunction with passive clip slings is designed for resident transfer in a homecare setting, at nursing homes and other assisted li
Terminated
FSANone listed
Feb 5, 2019Arjohuntleigh Magog
ARJOHUNTLEIGH GETINGE GROUP, RotoProne Therapy System, Model Number 209800
Terminated
IKZNone listed
Feb 12, 2018Arjohuntleigh Magog
Q-Connect 272 KG Scale used with Maxi Sky 2 ceiling lift The Scale is intended to be used with patient lifters to measure the weight of a patient who cannot stand on a scale. It is designed to be use
Terminated
FSANone listed
Feb 12, 2018Arjohuntleigh Magog
Quick Connect 272 KG Scale used with Maxi Sky 2 ceiling lift The Scale is intended to be used with patient lifters to measure the weight of a patient who cannot stand on a scale. It is designed to be
Terminated
FSANone listed
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