Data / Medical devices / Canada / Synthesis Health Intelligence Inc.
Synthesis Health Intelligence Inc.: FDA-registered device maker in Maple Ridge British Columbia, Canada, 1 510(k) clearance
Synthesis Health Intelligence Inc. is registered with the FDA (registration 3032579549) in Maple Ridge British Columbia, Canada. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 8, 2024. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3032579549
- Address
- 22420 Dewdney Trunk Rd Suite 300, Maple Ridge British Columbia, Canada, V2X 3J5
- Owner or operator
- Synthesis Health Intelligence Inc. (10091358)
- Roles
- Complaint file establishment, Manufacturer
- First device listed
- September 4, 2024
- Registered through
- 2026
- Brand names listed
- Synthesis "VISION" viewer
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Image Processing, Radiological | LLZ | 2 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| August 8, 2024 | K240724 | SynthVISION 1.0.0 | LLZ | Substantially Equivalent | Synthesis Health Intelligence, Inc. | accessdata.fda.gov |
Compare with other makers
Updated August 8, 2024. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.