Data / Medical devices / Canada / Ortho Attachyhook Supply Ltd.
Ortho Attachyhook Supply Ltd.: FDA-registered device maker in Anmore British Columbia, Canada, 1 510(k) clearance
Ortho Attachyhook Supply Ltd. is registered with the FDA (registration 3045079145) in Anmore British Columbia, Canada. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 7, 2019. 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
- 3045079145
- Address
- 2176 Summerwood Lane, Anmore British Columbia, Canada, V3H0G2
- Owner or operator
- Ortho Attachyhook Supply LTD. (10095747)
- Roles
- Exporter to the US, Foreign private label distributor, Specification developer
- First device listed
- April 23, 2026
- Registered through
- 2026
- Brand names listed
- Attachyhook Bracket, Attachyhook button, Ceramic Bracket
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bracket, Ceramic, Orthodontic | NJM | 2 | Exporter to the US, Foreign private label distributor, Specification developer | accessdata.fda.gov |
| Bracket, Metal, Orthodontic | EJF | 1 | Exporter to the US, Foreign private label distributor, Specification developer | accessdata.fda.gov |
| Setter, Band, Orthodontic | ECR | 1 | Exporter to the US, Foreign private label distributor, 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 7, 2019 | K180952 | Ceramic Bracket | NJM | Substantially Equivalent | Mem Dental Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Bracket, Ceramic, Orthodontic
- All makers of Bracket, Metal, Orthodontic
- All makers of Setter, Band, Orthodontic
Updated June 7, 2019. 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.