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KARMAN HEALTHCARE INC.

Last updated September 17, 2026

Information

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Device	Model / Reference	Registries	Class	Status
Karman Healthcare	LT-1000HB-BD	FDA UDI	Class I	Active
Karman Healthcare	KN-TV10A	FDA UDI	Class I	Active
Karman Healthcare	802N-DY	FDA UDI	Class I	Active
Karman Healthcare	XO-505-LUX	FDA UDI	Class II	Active
Karman Healthcare	T-922W	FDA UDI	Class I	Active
Karman Healthcare	XO-505-TB	FDA UDI	Class II	Active
Karman Healthcare	LT-770Q	FDA UDI	Class I	Active
Karman Healthcare	KN-924W-APT	FDA UDI	Class I	Active
Karman Healthcare	XO-202	FDA UDI	Class II	Active
Karman Healthcare	KN-880N-E	FDA UDI	Class I	Active
Karman Healthcare	PW-F500-SI	FDA UDI	Class II	Active
Karman Healthcare	KN-922W-APT	FDA UDI	Class I	Active
Karman Healthcare	XO-202N	FDA UDI	Class II	Active
Karman Healthcare	LT-700T-20W	FDA UDI	Class I	Active
Karman Healthcare	T-2017	FDA UDI	Class I	Active
Karman Wheelchair	K002202	FDA 510(k)	Class I	Active
Karman Wheelchair	K002167	FDA 510(k)	Class I	Active
Karma Wheelchair	K950195	FDA 510(k)	Class I	Active

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Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
Jan 27, 2016	Z-1025-2016	—	terminated	Karman Healthcare, Inc. is recalling Karma Flexx Wheelchair because incorrect size screws and corresponding hardware were installed on the front caster fork brackets.