510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K230548Substantially Equivalent

Myoaligner Appliance

Myohealth Technologies, LLC, Portland OR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K230548 is the FDA 510(k) clearance record for Myoaligner Appliance, cleared for Myohealth Technologies, LLC on under FDA product code MQC (Mouthguard, Prescription). FDA records list one 510(k) clearance for Myohealth Technologies, LLC. As of , FDA records show no recalls naming K230548.

Clearance record

Decision date
Received
(339 days to decision)
Product code
MQC Mouthguard, Prescription
Device class
Unclassified
Review panel
Unknown
Applicant
Myohealth Technologies, LLC 13765 NW Cornell Rd. Suite 150, Portland OR
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MQC

Trailing 12 months
2 clearances under product code MQC in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code MQC, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20260
March 20261
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260