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MONTERIS MEDICAL CORP

US

Last updated September 17, 2026

Information

Country
US
Address
131 Cheshire Lane, Suite 100, Minnetonka, MN, 55305
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
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EUDAMED SRN
—
FDA FEI Number
3009970070
DUNS Number
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Catalogue (182)

Page 1 of 4
DeviceModel / ReferenceRegistriesClassStatus
FullFire® Select Diffusing Tip Laser Probe 20624-4
FDA UDI
Class IIUnknown
AtamA™ System 20562
FDA UDI
Class IIUnknown
SideFire® Directional Laser Probe 20368-2
FDA UDI
Class IIUnknown
Mini-Bolt System 20817
FDA UDI
Class IActive
SideFire® Directional Laser Probe 20368-5
FDA UDI
Class IIUnknown
FullFire® Select Diffusing Tip Laser Probe 20624-3
FDA UDI
Class IIUnknown
Mini-Bolt System 20814
FDA UDI
Class IActive
NeuroBlate NB3 FullFire™ 1.6 Laser Probe 22002
FDA UDI
Class IIActive
Mini-Bolt System 20694
FDA UDI
Class IActive
Mini-Bolt System 20677
FDA UDI
Class IActive
Mini-Bolt System 20739
FDA UDI
Class IActive
Mini-Bolt System 20628
FDA UDI
Class IActive
Mini-Bolt System 20816
FDA UDI
Class IActive
AtamA™ System 20760
FDA UDI
Class IIActive
NeuroBlate Optic SideFire® Laser Probe 20891-2
FDA UDI
Class IIActive
NeuroBlate® System 20360
FDA UDI
Class IIUnknown
NeuroBlate Optic FullFire® Laser Probe 20895-00
FDA UDI
Class IIActive
FullFire® Diffusing Tip Laser Probe 20414-00
FDA UDI
Class IIUnknown
SideFire® Directional Laser Probe 20368-4
FDA UDI
Class IIUnknown
Mini-Bolt VUE Accessory Kit 21155
FDA UDI
Class IActive
Mini-Bolt System 20818
FDA UDI
Class IActive
Mini-Bolt System 21224
FDA UDI
Class IActive
FullFire® Select Diffusing Tip Laser Probe 20624-00
FDA UDI
Class IIUnknown
FullFire® Diffusing Tip Laser Probe 20414-00
FDA UDI
Class IIUnknown
FullFire® Diffusing Tip Laser Probe 20414-3
FDA UDI
Class IIUnknown
2.2mm Mini-Bolt 21100
FDA UDI
Class IActive
NeuroBlate® System 20720
FDA UDI
Class IIUnknown
Mini-Bolt System 20755
FDA UDI
Class IActive
FullFire® Diffusing Tip Laser Probe 20414-2
FDA UDI
Class IIUnknown
SideFire® Directional Laser Probe 20368-4
FDA UDI
Class IIUnknown
FullFire® Select Diffusing Tip Laser Probe 20624-1
FDA UDI
Class IIUnknown
Mini-Bolt System 21165
FDA UDI
Class IActive
Mini-Bolt System 20810
FDA UDI
Class IActive
Mini-Bolt System 20722
FDA UDI
Class IActive
NeuroBlate Optic FullFire® Laser Probe 20895-2
FDA UDI
Class IIActive
2.2mm Mini-Bolt VUE 21122
FDA UDI
Class IActive
NeuroBlate® System 20720
FDA UDI
Class IIUnknown
NeuroBlate Optic SideFire® Laser Probe 20891-4
FDA UDI
Class IIActive
AtamA™ System 20765
FDA UDI
Class IIActive
Mini-Bolt System 20815
FDA UDI
Class IActive
FullFire® Diffusing Tip Laser Probe 20414-1
FDA UDI
Class IIUnknown
NeuroBlate Optic FullFire® Laser Probe 20893-000
FDA UDI
Class IIActive
FullFire® Diffusing Tip Laser Probe 20414-00
FDA UDI
Class IIUnknown
NeuroBlate® System 20985
FDA UDI
Class IIActive
NeuroBlate® Robotic Probe Driver 20772
FDA UDI
Class IIActive
Mini-Bolt System 21237
FDA UDI
Class IActive
NeuroBlate Optic FullFire® Laser Probe 20893-1
FDA UDI
Class IIActive
NeuroBlate® Advanced Probe Driver 20369
FDA UDI
Class IIUnknown
FullFire® Diffusing Tip Laser Probe 20414-2
FDA UDI
Class IIUnknown
SideFire® Directional Laser Probe 20368-1
FDA UDI
Class IIUnknown

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FDA Recalls (4)

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
Oct 5, 2017Z-0194-2018—terminated

The firm received complaints that involved an unanticipated interaction between a NeuroBlate system and 1.5 Tesla (1.ST) MRI systems.

Mar 25, 2016Z-1614-2016—terminated

Monteris received a report that the sapphire lens on a 2.2SF probe fractured during a LITT procedure, with resulting introduction of C02 into the patient's brain.

Oct 3, 2014Z-0228-2015—terminated

Monteris Medical received a complaint of a separation of the distal sapphire tip from the laser delivery probe.

Oct 3, 2014Z-0227-2015—terminated

Monteris Medical received a complaint of a separation of the distal sapphire tip from the laser delivery probe.