RegWardenFDA facility compliance records
Facility

Conavi Medical Inc

1 recall(s) on record — most severe on record: Class I.

Activity by year

FDA actions on record by year2025: 1 recalls20172018201920202021202220232024120252026
  • Recalls (1)

Devices registered here (3)

  • System, Imaging, Optical Coherence Tomography (Oct)
    Product code NQQ (opens in a new tab) · Class II · Radiology · 21 CFR 892.1560
  • Catheter, Ultrasound, Intravascular
    Product code OBJ (opens in a new tab) · Class II · Cardiovascular · 21 CFR 870.1200
  • System, Imaging, Pulsed Echo, Ultrasonic
    Product code IYO (opens in a new tab) · Class II · Radiology · 21 CFR 892.1560

Recalls & enforcement

Related

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Conavi Medical Inc (FEI 3012198618) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3012198618-conavi-medical-inc/

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