# Conavi Medical Inc (specification developer, Toronto Ontario, CA): 3 new FDA device listings, incl. system, imaging, optical coherence tomography (oct)

**Score:** 75/100

| Field | Value |
|---|---|
| Establishment | Conavi Medical Inc |
| Owner / operator | Conavi Medical Inc. |
| Role | Specification developer (outsources manufacturing) |
| Establishment types | Develop Specifications But Do Not Manufacture At This Facility |
| Location | Toronto Ontario, CA |
| New listings | 3 |
| Devices | System, Imaging, Optical Coherence Tomography (Oct); System, Imaging, Pulsed Echo, Ultrasonic; Catheter, Ultrasound, Intravascular |
| Product codes | NQQ, IYO, OBJ |
| Device classes | Class II |
| Medical specialties | Radiology, Cardiovascular |
| Brand names | Novasight Hybrid System; Conavi IVUS OCT Hybrid Catheter |
| First new listing | 2026-09-11 |
| Latest new listing | 2026-09-11 |
| FDA registration number | 3012198618 |
| Registration expires | 2026-12-31 |

## Why this score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-10-28T20:51:27.468Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.