Data / Medical devices / Canada / CNTRL+ Inc.
CNTRL+ Inc.: FDA-registered device maker in Cornwall Ontario, Canada, 1 510(k) clearance
CNTRL+ Inc. is registered with the FDA (registration 3036802560) in Cornwall Ontario, Canada. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 17, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3036802560
- Address
- 127 Augustus St. Unit 1, Cornwall Ontario, Canada, K6J 3V9
- Owner or operator
- Cntrl+ Inc. (10092725)
- Roles
- Manufacturer
- First device listed
- February 11, 2025
- Registered through
- 2026
- Brand names listed
- Cntrl+ Bladder Support Pessary
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Pessary, Vaginal | HHW | 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 |
|---|---|---|---|---|---|---|
| December 17, 2024 | K240798 | Cntrl+ Bladder Support Pessary | HHW | Substantially Equivalent | Cntrl+, Inc. | accessdata.fda.gov |
Compare with other makers
Updated December 17, 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.