510(k) K260790
K260790 is an FDA 510(k) premarket notification submitted by ASESSO HEALTH, Inc. for the device "G-Series Grind Guard". The FDA issued a decision of Substantially Equivalent on June 25, 2026. The device falls under product code OBR (Mouthguard, Over-The-Counter), a Class U device.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 25, 2026
- Date Received
- March 11, 2026
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Mouthguard, Over-The-Counter
- Device Class
- Class U
- Regulation Number
- Review Panel
- DE
- Submission Type
To protect the teeth and reduce damage caused by bruxing or nighttime grinding and prevention of the noise associated with bruxing and grinding.