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Intraop Medical, Inc.

US

Last updated May 23, 2026

Information

Country
US
Address
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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
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DUNS Number
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Catalogue (2)

DeviceModel / ReferenceRegistriesClassStatus
Mobetron MOBETRON
FDA UDI
Class IIActive
Mobetron K981112
FDA 510(k)
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (1)

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
Jun 20, 2008Z-0014-2009—terminated

Docking screw/nut failure, which may result in a treatment head dropping, potentially impacting the patient.