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Sign in to claim this brandMONTERIS MEDICAL CORP
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 131 Cheshire Lane, Suite 100, Minnetonka, MN, 55305
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
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- FDA FEI Number
- 3009970070
- DUNS Number
- —
Catalogue (182)
Page 1 of 4| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| FullFire® Select Diffusing Tip Laser Probe | 20624-4 | FDA UDI | Class II | Unknown |
| AtamA™ System | 20562 | FDA UDI | Class II | Unknown |
| SideFire® Directional Laser Probe | 20368-2 | FDA UDI | Class II | Unknown |
| Mini-Bolt System | 20817 | FDA UDI | Class I | Active |
| SideFire® Directional Laser Probe | 20368-5 | FDA UDI | Class II | Unknown |
| FullFire® Select Diffusing Tip Laser Probe | 20624-3 | FDA UDI | Class II | Unknown |
| Mini-Bolt System | 20814 | FDA UDI | Class I | Active |
| NeuroBlate NB3 FullFire™ 1.6 Laser Probe | 22002 | FDA UDI | Class II | Active |
| Mini-Bolt System | 20694 | FDA UDI | Class I | Active |
| Mini-Bolt System | 20677 | FDA UDI | Class I | Active |
| Mini-Bolt System | 20739 | FDA UDI | Class I | Active |
| Mini-Bolt System | 20628 | FDA UDI | Class I | Active |
| Mini-Bolt System | 20816 | FDA UDI | Class I | Active |
| AtamA™ System | 20760 | FDA UDI | Class II | Active |
| NeuroBlate Optic SideFire® Laser Probe | 20891-2 | FDA UDI | Class II | Active |
| NeuroBlate® System | 20360 | FDA UDI | Class II | Unknown |
| NeuroBlate Optic FullFire® Laser Probe | 20895-00 | FDA UDI | Class II | Active |
| FullFire® Diffusing Tip Laser Probe | 20414-00 | FDA UDI | Class II | Unknown |
| SideFire® Directional Laser Probe | 20368-4 | FDA UDI | Class II | Unknown |
| Mini-Bolt VUE Accessory Kit | 21155 | FDA UDI | Class I | Active |
| Mini-Bolt System | 20818 | FDA UDI | Class I | Active |
| Mini-Bolt System | 21224 | FDA UDI | Class I | Active |
| FullFire® Select Diffusing Tip Laser Probe | 20624-00 | FDA UDI | Class II | Unknown |
| FullFire® Diffusing Tip Laser Probe | 20414-00 | FDA UDI | Class II | Unknown |
| FullFire® Diffusing Tip Laser Probe | 20414-3 | FDA UDI | Class II | Unknown |
| 2.2mm Mini-Bolt | 21100 | FDA UDI | Class I | Active |
| NeuroBlate® System | 20720 | FDA UDI | Class II | Unknown |
| Mini-Bolt System | 20755 | FDA UDI | Class I | Active |
| FullFire® Diffusing Tip Laser Probe | 20414-2 | FDA UDI | Class II | Unknown |
| SideFire® Directional Laser Probe | 20368-4 | FDA UDI | Class II | Unknown |
| FullFire® Select Diffusing Tip Laser Probe | 20624-1 | FDA UDI | Class II | Unknown |
| Mini-Bolt System | 21165 | FDA UDI | Class I | Active |
| Mini-Bolt System | 20810 | FDA UDI | Class I | Active |
| Mini-Bolt System | 20722 | FDA UDI | Class I | Active |
| NeuroBlate Optic FullFire® Laser Probe | 20895-2 | FDA UDI | Class II | Active |
| 2.2mm Mini-Bolt VUE | 21122 | FDA UDI | Class I | Active |
| NeuroBlate® System | 20720 | FDA UDI | Class II | Unknown |
| NeuroBlate Optic SideFire® Laser Probe | 20891-4 | FDA UDI | Class II | Active |
| AtamA™ System | 20765 | FDA UDI | Class II | Active |
| Mini-Bolt System | 20815 | FDA UDI | Class I | Active |
| FullFire® Diffusing Tip Laser Probe | 20414-1 | FDA UDI | Class II | Unknown |
| NeuroBlate Optic FullFire® Laser Probe | 20893-000 | FDA UDI | Class II | Active |
| FullFire® Diffusing Tip Laser Probe | 20414-00 | FDA UDI | Class II | Unknown |
| NeuroBlate® System | 20985 | FDA UDI | Class II | Active |
| NeuroBlate® Robotic Probe Driver | 20772 | FDA UDI | Class II | Active |
| Mini-Bolt System | 21237 | FDA UDI | Class I | Active |
| NeuroBlate Optic FullFire® Laser Probe | 20893-1 | FDA UDI | Class II | Active |
| NeuroBlate® Advanced Probe Driver | 20369 | FDA UDI | Class II | Unknown |
| FullFire® Diffusing Tip Laser Probe | 20414-2 | FDA UDI | Class II | Unknown |
| SideFire® Directional Laser Probe | 20368-1 | FDA UDI | Class II | Unknown |
Related Companies
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Authorities
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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.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Oct 5, 2017 | Z-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, 2016 | Z-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, 2014 | Z-0228-2015 | — | terminated | Monteris Medical received a complaint of a separation of the distal sapphire tip from the laser delivery probe. |
| Oct 3, 2014 | Z-0227-2015 | — | terminated | Monteris Medical received a complaint of a separation of the distal sapphire tip from the laser delivery probe. |