FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

Anti Snore Mouthpiece

K Number: K250028 · Decision Oct 3, 2025
Classifications
1
FEI Numbers
105
Registration Numbers
105
Same Product Code
212
Applicant Total
1
Review Days
270

Basic Information

Device Name
Anti Snore Mouthpiece
K Number
K250028
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.5570
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dongguan Yiyao Science & Technology Development Co., Ltd.
Date Received
January 6, 2025
Decision Date
October 3, 2025
Product Code
LRK
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LRK Device, Anti-Snoring

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LRK), ordered by most recent decision date.

View all