Is this your brand? Sign in to claim ownership.
Sign in to claim this brandMedical Cv, Inc.
United States·US-MF-000022350
Last updated May 23, 2026
What Medical Cv, Inc. makes
Medical Cv, Inc. manufactures cardiac annuloplasty systems, including the Northrup Universal Annuloplasty System Model 1000, which is used for mitral valve repair. The company also produces ablation devices under the AtriLaze brand, including malleable and surgical ablation probes, soft tissue ablation systems, and laser ablation systems designed for cardiac tissue modification. Additionally, they supply cardiac valve replacements, such as the Omniscience and Omnicarbon cardiac valves, intended for surgical implantation.
The company’s devices are regulated under the US Food and Drug Administration (FDA) as Class II and Class III medical devices, requiring premarket approval (PMA) or 510(k) clearance. These products are listed in the FDA’s regulatory databases, and the manufacturer is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What does Medical Cv, Inc. manufacture?
Medical Cv, Inc. produces cardiac annuloplasty systems like the Northrup Universal Annuloplasty System Model 1000 for mitral valve repair, ablation devices under the AtriLaze brand for cardiac tissue modification, and cardiac valve replacements including the Omniscience and Omnicarbon valves.
Where is Medical Cv, Inc. based?
Medical Cv, Inc. is based in the United States, as indicated by the country designation in their device registration information.
Which regulatory registries list Medical Cv, Inc.'s devices?
Medical Cv, Inc.'s devices are listed in the FDA's 510(k) clearance database and the Premarket Approval (PMA) database, reflecting their regulatory pathway for Class II and Class medical devices.
How are Medical Cv, Inc.'s devices classified?
Medical Cv, Inc.'s devices are classified as either Class II or Class III medical devices under FDA regulation, with Class II devices requiring 510(k) clearance and Class III devices requiring premarket approval (PMA).
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- United States
- Address
- 15002, North 25th Drive, Phoenix, AZ, United States
- Website
- www.icmedical.com
- —
- —
- [email protected]
- Phone
- +1 623 780 0700
- PRRC Contact
- Elena Simona Buiga
- EUDAMED SRN
- US-MF-000022350
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (200)
Page 3 of 4| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Crystal Vision | ICM-360-0000 | FDA UDI | Class II | Active |
| Non-Telescopic PenEvac® MaxReveal ™ Diamond Crystal® | ICM-000-0686 | FDA UDI | Class II | Active |
| Steris | SSEPET06 | FDA UDI | Class II | Unknown |
| Electrode | ICM-000-0334 | FDA UDI | Class II | Active |
| Ultra Vac | 3110-10EC | FDA UDI | Class II | Active |
| PenEvac1 | ICM-000-0545 | FDA UDI | Class II | Active |
| Non-Telescopic PenEvac | ICM-000-0592 | FDA UDI | Class II | Active |
| Steris | SSEPET03 | FDA UDI | Class II | Unknown |
| Non-Telescopic PenEvac | ICM-000-0580 | FDA UDI | Class II | Active |
| ESU Sensor | ICM-000-0009 | FDA UDI | Class II | Active |
| PenEvac1 | ICM-000-0478 | FDA UDI | Class II | Active |
| Steris | SSECAPREG | FDA UDI | Class II | Unknown |
| Steris | SSESEN02 | FDA UDI | Class II | Unknown |
| Laser Sensor | ICM-000-0018 | FDA UDI | Class II | Active |
| Smoke Tubing | ICM-000-0236 | FDA UDI | Class II | Active |
| PenEvac1 | ICM-000-0466 | FDA UDI | Class II | Active |
| Steris | SSEPET15 | FDA UDI | Class II | Unknown |
| PenEvac1 | ICM-000-0494 | FDA UDI | Class II | Active |
| ULPA Box Filter | ICM-000-0262 | EUDAMEDFDA UDI | Class II | Active |
| ESU Shroud | ICM-000-0542 | FDA UDI | Class II | Active |
| Crystal Vision | ICM-250-0000 | FDA UDI | Class II | Active |
| PenEvac1 | ICM-000-0541 | FDA UDI | Class II | Active |
| Ultra Vac E-Z Clean | 211010J | FDA UDI | Class II | Unknown |
| Smoke Evacuator Wand | ICM-000-0030 | EUDAMEDFDA UDI | Class II | Active |
| ULPA Filter & Water Trap | ICM-000-0307 | EUDAMEDFDA UDI | Class II | Active |
| PenEvac1 | ICM-000-0587 | FDA UDI | Class II | Active |
| Non-Telescopic PenEvac® MaxReveal ™ Diamond Crystal® | ICM-000-0716 | FDA UDI | Class II | Active |
| ESU Shroud | ICM-000-0101 | FDA UDI | Class II | Unknown |
| Electrode | ICM-000-0332 | FDA UDI | Class II | Active |
| Attacha Vac | 2120-09EC | FDA UDI | Class II | Unknown |
| Attacha Vac | 2120-09 | FDA UDI | Class II | Unknown |
| Ultra Vac E-Z Clean | 211010EC | FDA UDI | Class II | Unknown |
| Non-Telescopic PenEvac | ICM-000-0700 | FDA UDI | Class II | Active |
| Steris | SSEPEN03 | FDA UDI | Class II | Unknown |
| Steris | SSETUB01 | FDA UDI | Class II | Unknown |
| PenEvac1 | ICM-000-0674 | FDA UDI | Class II | Active |
| Attacha Vac | 212009J | FDA UDI | Class II | Unknown |
| PenEvac1 | ICM-000-0562 | FDA UDI | Class II | Active |
| Speculum Tubing | ICM-000-0365 | EUDAMEDFDA UDI | Class II | Active |
| Steris | SSEPEN14 | FDA UDI | Class II | Unknown |
| Non-Telescopic PenEvac | ICM-000-0544 | FDA UDI | Class II | Active |
| Non-Telescopic PenEvac | ICM-000-0591 | FDA UDI | Class II | Active |
| Steris | SSEPEN02 | FDA UDI | Class II | Unknown |
| RF Sensor, Shielded, 15 Feet | ICM-000-0561 | FDA UDI | Class II | Active |
| ESU Shroud | ICM-000-0357 | FDA UDI | Class II | Active |
| Smoke Tubing | ICM-000-0347 | EUDAMEDFDA UDI | Class II | Active |
| Non-Telescopic PenEvac | ICM-000-0534 | FDA UDI | Class II | Active |
| Electrode | ICM-000-0330 | FDA UDI | Class II | Active |
| Steris | SSEPEN12 | FDA UDI | Class II | Unknown |
| Non-Telescopic PenEvac® MaxReveal ™ Diamond Crystal® | ICM-000-0718 | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.
FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- IC Medical GmbH DE