FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Virtus

K Number: K261366 · Decision Jun 12, 2026
Classifications
1
FEI Numbers
105
Registration Numbers
105
Same Product Code
212
Applicant Total
11
Review Days
46

Basic Information

Device Name
Virtus
K Number
K261366
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
872.5570
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Somnomed, Inc.
Date Received
April 27, 2026
Decision Date
June 12, 2026
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

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Other Clearances by Somnomed, Inc.

K Number Device Name
K233497 Rest Assure System
K183443 SomnoDent Avant
K162306 SomnoDent ALPHA
K150369 SomnoDent Classic with DentiTrac Micro-recorder, SomnoDent Flex with DentiTrac Micro-recorder, SomnoDent Herbst Advance (Classic or Flex Retention) with DentiTrac Micro-recorder, SomnoDent G2 (Classic or Flex Retention) with DentiTrac Micro-recorder, SomnoDent Fusion (Classic or Flex Retention) with DentiTrac Micro-recorder
K140278 SOMNODENT FUSION, CLASSIC; SOMNODENT FUSION, FLEX
K130558 SOMNODENT HERBST; CLASSIC, FLEX
K121340 SOMNODENT G2
K102909 SOMNOBRUX SPLINTS
K102521 PANTINO PRO POSITINER
K073004 SOMNOMED BFLEX
Search all 11 clearances from Somnomed, Inc. →