Data / Medical devices / Finland / Stick Tech Ltd.
Stick Tech Ltd.: FDA-registered device maker in TURKU Pirkanmaa, Finland, 8 510(k) clearances
Stick Tech Ltd. is registered with the FDA (registration 9710611) in TURKU Pirkanmaa, Finland. It lists 5 device types. The FDA files 8 510(k) clearances under its listings, the newest dated March 21, 2006. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9710611
- FEI number
- 3003441270
- Address
- Lemminkaisenkatu 46, TURKU Pirkanmaa, Finland, FI-20521
- Owner or operator
- GC America Inc. (8030268)
- Roles
- Complaint file establishment, Manufacturer
- First device listed
- December 17, 2013
- Registered through
- 2026
- Brand names listed
- EVERSTICK A&O, EVERSTICK POST, Stick, StickNET, StickREFIX, everStickC&B, everStickNET, everStickORTHO and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bracket, Plastic, Orthodontic | DYW | 2 | Manufacturer | accessdata.fda.gov |
| Maintainer, Space Preformed, Orthodontic | DYT | 1 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Post, Root Canal | ELR | 1 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Protector, Silicate | EFX | 1 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Resin, Denture, Relining, Repairing, Rebasing | EBI | 2 | Complaint file establishment, 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 |
|---|---|---|---|---|---|---|
| March 21, 2006 | K051953 | EVERSTICK A&O | DYW | Substantially Equivalent | Stick Tech , Ltd. | accessdata.fda.gov |
| May 20, 2003 | K030820 | EVERSTICK POST | ELR | Substantially Equivalent | Stick Tech , Ltd. | accessdata.fda.gov |
| April 10, 2003 | K030072 | EVERSTICK PERIO | EBI | Substantially Equivalent | Stick Tech , Ltd. | accessdata.fda.gov |
| May 13, 2002 | K021126 | EVERSTICK ORTHO | EBI | Substantially Equivalent | Stick Tech , Ltd. | accessdata.fda.gov |
| November 5, 2001 | K011799 | EVERSTICKNET | EBI | Substantially Equivalent | Stick Tech , Ltd. | accessdata.fda.gov |
| November 5, 2001 | K011788 | EVERSTICK | EBI | Substantially Equivalent | Stick Tech , Ltd. | accessdata.fda.gov |
| January 8, 2001 | K003334 | STICK NET | EBI | Substantially Equivalent | Stick Tech , Ltd. | accessdata.fda.gov |
| January 4, 2001 | K003333 | STICK | EBI | Substantially Equivalent | Stick Tech , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Maintainer, Space Preformed, Orthodontic
- All makers of Resin, Denture, Relining, Repairing, Rebasing
- All makers of Post, Root Canal
- All makers of Protector, Silicate
- All makers of Bracket, Plastic, Orthodontic
Updated March 21, 2006. 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.