Data / Medical devices / Canada / Canadian Dry Storage Ltd.
Canadian Dry Storage Ltd.: FDA-registered device maker in Richmond British Columbia, Canada, 1 510(k) clearance
Canadian Dry Storage Ltd. is registered with the FDA (registration 3007617180) in Richmond British Columbia, Canada. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 16, 2018. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3007617180
- Address
- 18351 McCartney Way, Richmond British Columbia, Canada, V6W 0A1
- Owner or operator
- Canadian Dry Storage Ltd. (10091976)
- Roles
- Exporter to the US
- First device listed
- November 21, 2024
- Registered through
- 2026
- Brand names listed
- TheraBreath Dry Mouth Lozenges
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Saliva, Artificial | LFD | U | Exporter to the US | 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 |
|---|---|---|---|---|---|---|
| March 16, 2018 | K171542 | TheraBreath Dry Mouth Oral Rinse, TheraBreath Dry Mouth Lozenges | LFD | Substantially Equivalent | Dr. Harold Katz, LLC (Dba Therabreath | accessdata.fda.gov |
Compare with other makers
Updated March 16, 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.