Data / Medical devices / Canada / GlobeStar Systems, Inc
GlobeStar Systems, Inc: FDA-registered device maker in Toronto Ontario, Canada, 1 510(k) clearance
GlobeStar Systems, Inc is registered with the FDA (registration 3009595635) in Toronto Ontario, Canada. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated February 1, 2012. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3009595635
- Address
- 7 Kodiak Crescent Suite 100, Toronto Ontario, Canada, M3J 3E5
- Owner or operator
- Connexall USA, Inc. (10035909)
- Roles
- Manufacturer
- First device listed
- May 10, 2012
- Registered through
- 2026
- Brand names listed
- CNS-CARE-U, CNS-LITE, CNSPRO-U, Connexall Suite of Software Products
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Network And Communication, Physiological Monitors | MSX | 2 | 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 |
|---|---|---|---|---|---|---|
| February 1, 2012 | K112650 | CONNEXALL SUITE OF SOFTWARE PRODUCTS | MSX | Substantially Equivalent | Connexall USA, Inc. | accessdata.fda.gov |
Compare with other makers
Updated February 1, 2012. 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.