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Blackrock Microsystems

US

Last updated September 17, 2026

Information

Country
US
Address
630 S Komas Dr Ste 200, Salt Lake City, UT, 84108
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
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EUDAMED SRN
—
FDA FEI Number
3007323246
DUNS Number
—

Catalogue (119)

Page 1 of 3
DeviceModel / ReferenceRegistriesClassStatus
Blackrock NeuroPort Biopotential Signal Processing System 9650
FDA UDI
Class IIActive
Blackrock NeuroPort Biopotential Signal Processing System 6.5.4
FDA UDI
Class IIUnknown
XactStrip 027682
FDA UDI
Class IIActive
Blackrock NeuroPort Biopotential Signal Processing System 8282
FDA UDI
Class IIActive
Digital NeuroPort Biopotential Signal Processing System 10908
FDA UDI
Class IIActive
XactGrid 027676
FDA UDI
Class IIActive
Blackrock NeuroPort Biopotential Signal Processing System 7.7.0
FDA UDI
Class IIActive
XactTrode Patient Cable 028896
FDA UDI
Class IIActive
XactTrode Patient Cable 028900
FDA UDI
Class IIActive
Blackrock NeuroPort Biopotential Signal Processing System 7121
FDA UDI
Class IIActive
XactGrid 027675
FDA UDI
Class IIActive
Digital NeuroPort Biopotential Signal Processing System 11058
FDA UDI
Class IIActive
XactTrode Patient Cable 029453
FDA UDI
Class IIActive
XactTrode Patient Cable 028906
FDA UDI
Class IIActive
Blackrock NeuroPort Biopotential Signal Processing System 7.0.4
FDA UDI
Class IIUnknown
XactTrode Patient Cable 028912
FDA UDI
Class IIActive
XactTrode Patient Cable 028903
FDA UDI
Class IIActive
Digital NeuroPort Biopotential Signal Processing System 13178
FDA UDI
Class IIActive
Digital NeuroPort Biopotential Signal Processing System 12125
FDA UDI
Class IIActive
XactStrip 028942
FDA UDI
Class IIActive
XactTrode Patient Cable 028916
FDA UDI
Class IIActive
XactStrip 027684
FDA UDI
Class IIActive
NeuroPort Electrode (SIROF) 6248
FDA UDI
Class IIActive
Digital NeuroPort Biopotential Signal Processing System 10906
FDA UDI
Class IIActive
XactStrip 028936
FDA UDI
Class IIActive
Digital NeuroPort Biopotential Signal Processing System 12126
FDA UDI
Class IIActive
XactGrid 027690
FDA UDI
Class IIActive
Digital NeuroPort Biopotential Signal Processing System 10909
FDA UDI
Class IIActive
NeuroPort Electrode 4382
FDA UDI
Class IIActive
Digital NeuroPort Biopotential Signal Processing System 10480
FDA UDI
Class IIActive
Blackrock NeuroPort Biopotential Signal Processing System 7.6.0
FDA UDI
Class IIUnknown
Blackrock NeuroPort Biopotential Signal Processing System 7.6.1
FDA UDI
Class IIActive
XactGrid 027678
FDA UDI
Class IIActive
Blackrock NeuroPort Biopotential Signal Processing System 7.0.0
FDA UDI
Class IIUnknown
XactGrid 028943
FDA UDI
Class IIActive
XactStrip 028939
FDA UDI
Class IIActive
XactTrode Patient Cable 028902
FDA UDI
Class IIActive
Blackrock NeuroPort Biopotential Signal Processing System 6735
FDA UDI
Class IIUnknown
XactTrode Patient Cable 028634
FDA UDI
Class IIActive
XactTrode Patient Cable 028905
FDA UDI
Class IIActive
XactGrid 027691
FDA UDI
Class IIActive
XactStrip 027672
FDA UDI
Class IIActive
NeuroPort Inserter Assembly 4523
FDA UDI
Class IIActive
Blackrock NeuroPort Biopotential Signal Processing System 7.5.0
FDA UDI
Class IIUnknown
XactGrid 027686
FDA UDI
Class IIActive
Digital NeuroPort Biopotential Signal Processing System 13177
FDA UDI
Class IIActive
XactGrid 027680
FDA UDI
Class IIActive
XactGrid 027679
FDA UDI
Class IIActive
XactStrip 028935
FDA UDI
Class IIActive
Blackrock NeuroPort Biopotential Signal Processing System 10104
FDA UDI
Class IIActive

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FDA Recalls (2)

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

DateRecall No.ClassStatusReason
Aug 10, 2016Z-2764-2016—terminated

Blackrock Microsystems, LLC announces a voluntary field action for the Blackrock NeuroPort Biopotential Signal Processing System because the Neural Signal Amplifier and the Patient Cable are incorrectly labeled as Type CF Applied Parts.

Aug 10, 2016Z-2763-2016—terminated

Blackrock Microsystems, LLC announces a voluntary field action for the Blackrock NeuroPort Biopotential Signal Processing System because the Neural Signal Amplifier and the Patient Cable are incorrectly labeled as Type CF Applied Parts.