Data / Medical devices / Canada / Camden Passage
Camden Passage: FDA-registered device maker in Collingwood Ontario, Canada, 1 510(k) clearance
Camden Passage is registered with the FDA (registration 3013785060) in Collingwood Ontario, Canada. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 17, 2013. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3013785060
- Address
- 4 Georgian Court, Collingwood Ontario, Canada, L9Y4W5
- Owner or operator
- Camden Passage (10055878)
- Roles
- Specification developer
- First device listed
- July 11, 2018
- Registered through
- 2026
- Brand names listed
- Loox
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lenses, Soft Contact, Daily Wear | LPL | 2 | Specification developer | 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 17, 2013 | K123431 | DREAM COLOR I (POLYMACON) SOFT (HYDROPHILIC) CONTACT LENS, DREAM COLOR II (POLYMACON) SOFT (HYDROPHILIC) CONTACT LENS, D | LPL | Substantially Equivalent | Dreamcon Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated June 17, 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.