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Conavi Medical Inc

Last updated May 30, 2026

Information

Device	Model / Reference	Registries	Class	Status
Novasight Hybrid™ Catheter PIM Bag	SA-10-0029	FDA UDI	Class II	Active
Novasight Hybrid™ Catheter Accessories Package	SA-10-0022	FDA UDI	Class II	Active
Novasight Hybrid™ Hummingbird Console	TA-03-0005	FDA UDI	Class II	Active
Foresight ICE™ Catheter Accessories Package	SA-01-0015	FDA UDI	Class II	Active
Foresight ICE™ Catheter	TA-01-0001	FDA UDI	Class II	Active
Novasight Hybrid™ PIM	TA-07-0001	FDA UDI	Class II	Active
Foresight ICE™ PIM	TA-02-0001	FDA UDI	Class II	Active
Foresight ICE™ Hummingbird Console	TA-03-0001	FDA UDI	Class II	Active
Novasight Hybrid™ PIM	TA-07-0002	FDA UDI	Class II	Unknown
Novasight Hybrid™ Catheter	TA-06-0001	FDA UDI	Class II	Active
Novasight Hybrid™ Catheter	TA-06-0001	FDA UDI	Class II	Active
Novasight Hybrid System	K252945	FDA 510(k)	Class II	Active
Foresight Intracardiac Echocardiology (ICE) System	K162789	FDA 510(k)	Class II	Active
Novasight Hybrid System	K172258	FDA 510(k)	Class II	Active

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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
Mar 12, 2025	Z-1585-2025	—	open, classified	Due to manufacturing issues there is a potential for the catheter sheath to detach.

Establishments registered with the FDA under this company group, matched by name.