The following data is part of a premarket notification filed by Joel Lander D.d.s. with the FDA for Tooth Slooth.
| Device ID | K833338 |
| 510k Number | K833338 |
| Device Name: | TOOTH SLOOTH |
| Classification | Handle, Instrument, Dental |
| Applicant | JOEL LANDER D.D.S. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | EJB |
| CFR Regulation Number | 872.4565 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-09-27 |
| Decision Date | 1983-11-25 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() TOOTH SLOOTH 78740383 3150928 Live/Registered |
Professional Results, Inc. 2005-10-25 |
![]() TOOTH SLOOTH 73460656 1307891 Dead/Cancelled |
Tooth Slooth 1984-01-13 |