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Alcor Scientific

United States·US-MF-000029295

Last updated June 8, 2026

Information

Device	Model / Reference	Registries	Class	Status
Alcor SENTINELplus	EN-500SP	FDA UDI	Class II	Unknown
Alcor SENTINELplus	E-500SP	FDA UDI	Class II	Unknown
Alcor SENTINELplus	E-1004SP	FDA UDI	Class II	Unknown
Alcor SENTINELplus	E-1203SP	FDA UDI	Class II	Unknown
iSED Elite	112-00222	FDA UDI	Class I	Active
Sentinel®	S-2000-6	FDA UDI	Class II	Active
Alcor SENTINELplus	EN-1203SP	FDA UDI	Class II	Unknown
Sentinel®	S-2000-10	FDA UDI	Class II	Active
Alcor SENTINELplus	E-1004SP	FDA UDI	Class II	Unknown
Alcor SENTINELplus	E-1200SP	FDA UDI	Class II	Unknown
Alcor SENTINELplus	E-1203SP	FDA UDI	Class II	Unknown
Alcor SENTINELplus	EN-1004SP	FDA UDI	Class II	Unknown
Alcor SENTINELplus	EN-1203SP	FDA UDI	Class II	Unknown
Alcor SENTINELplus	EN-1200SP	FDA UDI	Class II	Unknown
Alcor SENTINELplus	EN-1200SP	FDA UDI	Class II	Unknown
Alcor SENTINELplus	E-1200SP	FDA UDI	Class II	Unknown
Alcor SENTINELplus	EN-500SP	FDA UDI	Class II	Unknown
Alcor SENTINELplus	E-500SP	FDA UDI	Class II	Unknown
Alcor SENTINELplus	EN-1004SP	FDA UDI	Class II	Active
Sentinel®	S-1000-SI	FDA UDI	Class II	Active
SENTINELplus	S-3000-IU	EUDAMEDFDA UDI	Class IIa	Active
miniiSED	112-01017	EUDAMEDFDA UDI	Class A	Active
iSED PRO	112-00120-SYS	EUDAMED	Class A	Active
iSED	112-00101	EUDAMEDFDA UDI	Class A	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
Jul 20, 2022	Z-1751-2022	—	open, classified	Primary Pump Tubing Spare Part is incorrect. If the tubing is installed onto an ALCOR iSED ESR Analyzer, there is a potential of a biohazard leak from the iSEDs Probe Tube