EVERSTICK
Resin, Denture, Relining, Repairing, Rebasing
STICK TECH LTD.
The following data is part of a premarket notification filed by Stick Tech Ltd. with the FDA for Everstick.
Pre-market Notification Details
| Device ID | K011788 |
| 510k Number | K011788 |
| Device Name: | EVERSTICK |
| Classification | Resin, Denture, Relining, Repairing, Rebasing |
| Applicant | STICK TECH LTD. 80 PARKWAY WEST Mount Vernon, NY 10552 |
| Contact | William M Troetel |
| Correspondent | William M Troetel STICK TECH LTD. 80 PARKWAY WEST Mount Vernon, NY 10552 |
| Product Code | EBI |
| CFR Regulation Number | 872.3760 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2001-06-08 |
| Decision Date | 2001-11-05 |
| Summary: | summary |
NIH GUDID Devices
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00842092112632 | K011788 | 000 |
| 15400556008710 | K011788 | 000 |
| 15400556008703 | K011788 | 000 |
Trademark Results [EVERSTICK]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 EVERSTICK 76278417 2879900 Live/Registered |
Stick Tech Oy 2001-06-29 |
 EVERSTICK 71565763 0525271 Dead/Expired |
EVERSTICK ANCHOR COMPANY 1948-09-24 |
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