Ventripoint Diagnostics Ltd.
Toronto Ontario, CA
VENTRIPOINT DIAGNOSTICS LTD. appears in FDA device records in Toronto Ontario, CA. FDA records list 3 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 3 510(k) clearances for Ventripoint Diagnostics Ltd. between 2018 and 2025. The busiest year on record is 2018, with 1. The most recent is 2025, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2018 | 1 |
| 2019 | 1 |
| 2025 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K241222 | Ventripoint Medical System Plus (VMS+) 4.0 | QIH | Substantially Equivalent | |
| K191493 | Ventripoint Medical System Plus (VMS+) 3.0 | LLZ | Substantially Equivalent | |
| K173810 | Ventripoint Medical System Plus (VMS+) | IYN | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3007194257 | 3007194257 | VENTRIPOINT DIAGNOSTICS LTD. | 18 Hook Avenue, Toronto Ontario M6P1T4 CA | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain