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MICHIGAN INSTRUMENTS

US

Last updated September 17, 2026

Information

Country
US
Address
4717 Talon Ct SE, Grand Rapids, MI, 49512
Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
1821850
DUNS Number
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Catalogue (10)

DeviceModel / ReferenceRegistriesClassStatus
Thumper 1007CCMII
FDA UDI
Class IIActive
Thumper 1007CCV
FDA UDI
Class IIUnknown
Life-Stat 1008MII
FDA UDI
Class IIActive
Thumper Cardiopulmonary Resuscitator 1005 K851139
FDA 510(k)
Class IIActive
Cardiopulmunary Resuscitator K811909
FDA 510(k)
Class IIActive
Thumper Cardiopulmonary Resuscitator K962237
FDA 510(k)
Class IIActive
Thumper K972525
FDA 510(k)
Class IIActive
Cardiopulmonary Resuscitator K833879
FDA 510(k)
Class IIActive
Laryngostat Laryngoscope Handle K895954
FDA 510(k)
Class IActive
Thumper, Model: 1008 K073079
FDA 510(k)
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

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Notified Bodies

Not available yet.

Authorities

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FDA Recalls (3)

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
Feb 13, 2018Z-1632-2018—terminated

A performance issue with the chest depth needle valve (CDNV) may arise where turning the knob will not deliver any compression depth to the piston during the first 5 revolutions of the knob.The last to revolution of the knob could deliver a full 8cm of compression.

Sep 14, 2006Z-0178-2007—terminated

Failure to initiate compressions when turned on.

Aug 4, 2006Z-0119-2007—terminated

Failure to initiate compressions when first turned on, if improperly shut down-Operator Manual updated to include proper shut down procedures