Data / Medical devices / Canada / Synca Marketing
Synca Marketing: FDA-registered device maker in Repentigny Quebec, Canada, 4 510(k) clearances
Synca Marketing is registered with the FDA (registration 3006697692) in Repentigny Quebec, Canada. It lists 6 device types. The FDA files 4 510(k) clearances under its listings, the newest dated November 23, 2010. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3006697692
- Address
- 337 Marion St, Repentigny Quebec, Canada, J5Z 4W8
- Owner or operator
- Synca Marketing (10034495)
- Roles
- Exporter to the US, Repackager or relabeler
- First device listed
- December 6, 2010
- Registered through
- 2026
- Brand names listed
- Biolight Advanced Fiber Post, Biolight Drill Free, Biolight Dual kit, Biolight Dual reamer #0.5, Biolight Dual reamer #1, Biolight Dual reamer #2, Biolight Dual reamer #3, Biolight Dual refill #0.5 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Adhesive, Bracket And Tooth Conditioner, Resin | DYH | 2 | Exporter to the US | accessdata.fda.gov |
| Instruments, Dental Hand | DZN | 1 | Exporter to the US | accessdata.fda.gov |
| Loupe, Diagnostic/Surgical | FSP | 1 | Exporter to the US | accessdata.fda.gov |
| Post, Root Canal | ELR | 1 | Repackager or relabeler | accessdata.fda.gov |
| Resin, Denture, Relining, Repairing, Rebasing | EBI | 2 | Exporter to the US, Repackager or relabeler | accessdata.fda.gov |
| System, Image Processing, Radiological | LLZ | 2 | Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| November 23, 2010 | K102207 | FIBER FORCE | EBI | Substantially Equivalent | Synca Marketing, Inc. | accessdata.fda.gov |
| January 17, 2008 | K072978 | TENDER ORTHO BOND-ENA BOND-ENA ETCH | DYH | Substantially Equivalent | Micerium S.P.A. | accessdata.fda.gov |
| January 12, 2007 | K063170 | TENDER FIBER | EBI | Substantially Equivalent | Micerium S.P.A. | accessdata.fda.gov |
| November 20, 2006 | K062237 | CADI, VERSION 4 | LLZ | Substantially Equivalent | Synca Marketing, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Resin, Denture, Relining, Repairing, Rebasing
- All makers of Loupe, Diagnostic/Surgical
- All makers of Instruments, Dental Hand
- All makers of System, Image Processing, Radiological
- All makers of Adhesive, Bracket And Tooth Conditioner, Resin
- All makers of Post, Root Canal
Updated November 23, 2010. 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.