Data / Medical devices / Canada / Exciton Technologies Inc.
Exciton Technologies Inc.: FDA-registered device maker in Edmonton Alberta, Canada, 3 510(k) clearances
Exciton Technologies Inc. is registered with the FDA (registration 3007963765) in Edmonton Alberta, Canada. It lists 1 device type. The FDA files 3 510(k) clearances under its listings, the newest dated December 6, 2018. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3007963765
- Address
- Suite 4147 10230 Jasper Avenue, Edmonton Alberta, Canada, T5J 4P6
- Owner or operator
- Exciton Technologies Inc. (10030601)
- Roles
- Manufacturer
- First device listed
- January 7, 2013
- Registered through
- 2026
- Brand names listed
- KerraCel Ag Gelling Fiber Silver Dressing, exsalt CMC Gelling Fiber Dressing, exsalt PT7 Contact Layer, exsalt T7 Wound Dressing
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Dressing, Wound, Drug | FRO | U | 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 6, 2018 | K182680 | KerraContact Ag Perf Advanced Perforated Silver Wound Dressing | FRO | Substantially Equivalent | Exciton Technologies, Inc. | accessdata.fda.gov |
| February 13, 2017 | K162508 | KerraCel Ag Gelling Fiber Silver Dressing | FRO | Substantially Equivalent | Exciton Technologies, Inc. | accessdata.fda.gov |
| December 15, 2011 | K113564 | EXSALT T7 WOUND DRESSING | FRO | Substantially Equivalent | Exciton Technologies, Inc. | accessdata.fda.gov |
Compare with other makers
Updated December 6, 2018. 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.