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Beeken Biomedical

Last updated May 23, 2026

Information

Device	Model / Reference	Registries	Class	Status
NuStat Trauma Pad XR	XR-0404	FDA UDI	U	Active
NuStat Trauma Pad XR	XR-0812	FDA UDI	U	Active
NuStat Flex XR	3000097318	FDA UDI	U	Unknown
NuStat XR	XR-0408	FDA UDI	U	Active
NuStat Trauma Pad XR	XR-0812-5	FDA UDI	U	Unknown
NuStat	NS-0404	FDA UDI	U	Active
NuStat	N-0404NT	FDA UDI	U	Active
NuStat Tactical	NT-0236	FDA UDI	U	Unknown
NuStat Flex XR	XR-3000097331	FDA UDI	U	Active
NuStat Flex XR	XR-3000097317	FDA UDI	U	Active
NuStat Flex XR	XR-3000097333	FDA UDI	U	Active
NuStat	N-0404-1	FDA UDI	U	Unknown
NuStat Trauma Pad	N-0236	FDA UDI	U	Active
NuStat Flex XR	3000097317	FDA UDI	U	Unknown
NuStat Trauma Pad XR	XR-0448	FDA UDI	U	Active
NuStat	N-0404-2	FDA UDI	U	Unknown
NuStat Flex XR	3000097319	FDA UDI	U	Unknown
NuStat Flex XR	XR-3000097320	FDA UDI	U	Active
NuStat Flex	XR-0348	FDA UDI	U	Active
NuStat Flex XR	3000097331	FDA UDI	U	Unknown
NuStat Flex XR	3000097333	FDA UDI	U	Unknown
NuStat Trauma Pad XR	XR-0404-5	FDA UDI	U	Unknown
NuStat Flex XR	3000097320	FDA UDI	U	Unknown
Nustat, Nustat Xr	K142363	FDA 510(k)	U	Active
Nustat XR	K160578	FDA 510(k)	U	Active
NuStat	K183190	FDA 510(k)	Class II	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
Oct 14, 2021	Z-0309-2022	—	open, classified	Endotoxin levels exceeded allowable limits.