510(k) K243752

Device
Double Tube Herbst Appliance
Applicant
The Tmj Clinic PC
510(k) number
K243752
Product code
LRK
Decision
Substantially Equivalent (SESE)
Decision date
2025-09-17
Date received
2024-12-05
Regulation
872.5570
Classification name
Device, Anti-Snoring
Medical specialty
Dental
Review panel
Dental
Device class
2
Clearance type
Abbreviated
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
John Summer
Address
833 SW 11th Ave. # 810 Portland OR US 97205 97205

FDA Registration Numbers

Source Documents

510(k) summary PDF

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