Data / Medical devices / Canada / CHX Technologies Inc.
CHX Technologies Inc.: FDA-registered device maker in TORONTO Ontario, Canada, 1 510(k) clearance
CHX Technologies Inc. is registered with the FDA (registration 9680945) in TORONTO Ontario, Canada. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 25, 2002. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9680945
- FEI number
- 3002989672
- Address
- 3080 Yonge Street Suite 6060, TORONTO Ontario, Canada, M4N 3N1
- Owner or operator
- CHX TECHNOLOGIES, INC. (9012518)
- Roles
- Manufacturer
- First device listed
- February 28, 1995
- Registered through
- 2026
- Brand names listed
- PREVORA STAGE 2
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Varnish, Cavity | LBH | 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 |
|---|---|---|---|---|---|---|
| November 25, 2002 | K023671 | AQUEOUS ACRYLIC DISPERSION 28% W/W | LBH | Substantially Equivalent | Chx Technologies, Inc. | accessdata.fda.gov |
Compare with other makers
Updated November 25, 2002. 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.