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Sign in to claim this brandNeo Medical Inc.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 249 Freeport Blvd, Sparks, NV, 89431
- Website
- neomedicalinc.com
- —
- —
- [email protected]
- Phone
- 888-450-3334
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3007207906
- DUNS Number
- 015510540
Catalogue (302)
Page 1 of 7| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Neo Medical Cage kit | CP-13-22-AS | FDA UDI | Class II | Active |
| Neo Medical Pedicle screw kit | RD-00-50-ST | FDA UDI | Class II | Active |
| Neo Medical Pedicle Screw System | SI-PM-40-00 | FDA UDI | Class I | Active |
| Neo Medical Cage kit | CI-SD-11-00 | FDA UDI | Class I | Active |
| V-Cath | 304-166 | FDA UDI | Class II | Active |
| Neo Medical Cage kit | AS-26-13-00 | FDA UDI | Class II | Active |
| Neo Medical Pedicle screw kit | SI-PR-00-NS | FDA UDI | Class I | Active |
| NeoMagic | 3929-2650 | FDA UDI | Class II | Active |
| Neo Medical Cage kit | CI-SD-07-XL | FDA UDI | Class I | Active |
| Neo Medical Pedicle screw kit | SC-10-70-IL | FDA UDI | Class II | Active |
| Neo Medical Pedicle Screw System | SD-00-00-SS | FDA UDI | Class I | Active |
| PowerStick | 30101-1610 | FDA UDI | Class II | Active |
| Neo Medical Cage kit | AS-32-07-00 | FDA UDI | Class II | Active |
| NeoMagic | 2525-2650 | FDA UDI | Class II | Active |
| NeoMagic | 1944-1630 | FDA UDI | Class II | Active |
| Neo Medical Cage kit | AS-32-11-00 | FDA UDI | Class II | Active |
| Neo Medical Pedicle screw kit | SC-50-50-PE | FDA UDI | Class II | Active |
| Neo Medical Pedicle screw kit | RD-01-30-ST | FDA UDI | Class II | Active |
| Neo Medical Cage kit | AC-32-07-05 | FDA UDI | Class II | Active |
| NeoMagic | 3053-003 | FDA UDI | Class II | Active |
| Neo Medical Cage kit | AC-36-10-05 | FDA UDI | Class II | Active |
| Neo Medical Pedicle screw kit | RD-00-40-PB | FDA UDI | Class II | Active |
| NeoMagic | 3091-1640 | FDA UDI | Class II | Active |
| NeuroTrace | 553-23-02 | FDA UDI | Class II | Active |
| Neo Medical Cage kit | AS-32-13-00 | FDA UDI | Class II | Active |
| Neo Medical Cage kit | CI-00-TL-00 | FDA UDI | Class I | Active |
| Neo Medical Pedicle Screw System | KW-00-00-01 | FDA UDI | Class I | Active |
| NeoMagic | 4029-1660 | FDA UDI | Class II | Active |
| V-Cath | 500-008 | FDA UDI | Class II | Active |
| NeuroTrace | 557-18-05 | FDA UDI | Class II | Active |
| V-Cath | 380-75 | FDA UDI | Class II | Active |
| NeoMagic | 3525-262 | FDA UDI | Class II | Active |
| Neo Medical Cage kit | CP-07-22-AS | FDA UDI | Class II | Active |
| Neo Medical Cage kit | AS-26-07-00 | FDA UDI | Class II | Active |
| Neo Pedicle Screw System | SC-45-30-PE | FDA UDI | Class II | Active |
| NeoMagic | 1946-1606 | FDA UDI | Class II | Active |
| NeoMagic | 360-300 | FDA UDI | Class II | Active |
| Neo Medical Cage kit | CI-00-CP-01 | FDA UDI | Class I | Active |
| NeoMagic | 1943-1608 | FDA UDI | Class II | Active |
| Neo Pedicle Screw System | RD-05-00-CR | FDA UDI | Class II | Active |
| V-Cath | 407-166 | FDA UDI | Class II | Active |
| Neo Medical Pedicle screw kit | SC-70-35-PE | FDA UDI | Class II | Active |
| Neo Pedicle Screw System | CO-00-00-PA | FDA UDI | Class II | Active |
| NeoMagic | 3525-162 | FDA UDI | Class II | Active |
| Neo Medical Cage kit | CI-SD-13-00 | FDA UDI | Class I | Active |
| V-Cath | 360-25 | FDA UDI | Class II | Active |
| NeoMagic | 3025-162 | FDA UDI | Class II | Active |
| PowerStick | 30101-1608 | FDA UDI | Class II | Active |
| Neo Pedicle Screw System | SC-80-45-PE | FDA UDI | Class II | Active |
| Neo Medical Cage kit | CI-00-BC-00 | FDA UDI | Class I | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
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Notified Bodies
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Authorities
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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.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Apr 5, 2011 | Z-2223-2011 | — | terminated | Firm received recall notice from their contract manufacturer due to visible particulates in Bacteriostatic Sodium Chloride Injection, USP 0.9%, 30 mL vials that are included in insertion kits. |