Data / Medical devices / Canada / Zolar Technology & MFG Co Inc
Zolar Technology & MFG Co Inc: FDA-registered device maker in Mississauga Ontario, Canada, 1 510(k) clearance
Zolar Technology & MFG Co Inc is registered with the FDA (registration 3010364538) in Mississauga Ontario, Canada. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 5, 2013. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3010364538
- Address
- 1200 Derry Road East Unit # 5, Mississauga Ontario, Canada, L5T OB3
- Owner or operator
- Zolar Technology & Mfg Co Inc (10044494)
- Roles
- Manufacturer
- First device listed
- June 19, 2013
- Registered through
- 2026
- Brand names listed
- Cutting Fiber Kit, Disposable Tips, Pain Therapy Tip, Photon, Photon EXE, Photon Plus, Photon Plus EXE
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Powered Laser Surgical Instrument | GEX | 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 |
|---|---|---|---|---|---|---|
| June 5, 2013 | K122020 | PHOTON PHOTON PLUS | GEX | Substantially Equivalent | Zolar Technology & Mfg Co., Inc. | accessdata.fda.gov |
Compare with other makers
Updated June 5, 2013. 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.