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

SOMNODENT G2

K Number: K121340 · Decision May 30, 2012
Classifications
1
FEI Numbers
105
Registration Numbers
105
Same Product Code
212
Applicant Total
11
Review Days
27

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
SOMNODENT G2
K Number
K121340
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.5570
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Somnomed, Inc.
Date Received
May 3, 2012
Decision Date
May 30, 2012
Product Code
LRK
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
Y

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

Other Clearances by Somnomed, Inc.

K Number Device Name
K261366 Virtus
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
K102909 SOMNOBRUX SPLINTS
K102521 PANTINO PRO POSITINER
K073004 SOMNOMED BFLEX
Search all 11 clearances from Somnomed, Inc. →