Data / Medical devices / Canada / Innovative Excimer Solutions, Inc.
Innovative Excimer Solutions, Inc.: FDA-registered device maker in Toronto Ontario, Canada, 1 510(k) clearance
Innovative Excimer Solutions, Inc. is registered with the FDA (registration 8043867) in Toronto Ontario, Canada. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated January 9, 1997. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 8043867
- FEI number
- 3001126113
- Address
- 136 Sparks Avenue, Toronto Ontario, Canada, M2H 2S4
- Owner or operator
- INNOVATIVE EXCIMER SOLUTIONS, INC. (9004212)
- Roles
- Manufacturer
- First device listed
- November 15, 2007
- Registered through
- 2026
- Brand names listed
- Amoils Epithelial Scrubber
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Burr, Corneal, Battery-Powered | HOG | 1 | 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 |
|---|---|---|---|---|---|---|
| January 9, 1997 | K962989 | AMOILS EPITHELIAL SCRUBBER | HOG | Substantially Equivalent | S. Percy Amoils | accessdata.fda.gov |
Compare with other makers
Updated January 9, 1997. 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.