The following data is part of a premarket notification filed by Grind Guard Technologies, Llc with the FDA for Grindguard.
Device ID | K082723 |
510k Number | K082723 |
Device Name: | GRINDGUARD |
Classification | Mouthguard, Prescription |
Applicant | GRIND GUARD TECHNOLOGIES, LLC 342 E. MAIN STREET SUITE 207 Leola, PA 17540 |
Contact | Bill Mclain |
Correspondent | Bill Mclain GRIND GUARD TECHNOLOGIES, LLC 342 E. MAIN STREET SUITE 207 Leola, PA 17540 |
Product Code | MQC |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2008-09-17 |
Decision Date | 2009-08-31 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
GRINDGUARD 98008375 not registered Live/Pending |
Hambli Limited 2023-05-23 |
GRINDGUARD 85177835 not registered Dead/Abandoned |
Medtech Products Inc. 2010-11-16 |
GRINDGUARD 77403738 not registered Dead/Abandoned |
Pelerin, Joseph J. 2008-02-22 |
GRINDGUARD 75082108 not registered Dead/Abandoned |
JAKSIC, BRYANT J. 1996-04-01 |