FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

BRUX MOUTHGUARDS

K Number: K111310 · Decision Dec 8, 2011
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
44
Applicant Total
2
Review Days
212

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Basic Information

Device Name
BRUX MOUTHGUARDS
K Number
K111310
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dental Arte, Inc.
Date Received
May 10, 2011
Decision Date
December 8, 2011
Product Code
OBR
Advisory Committee
Unknown
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
OBR Mouthguard, Over-The-Counter

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K Number Device Name
K060086 FENIIIIIIX COLORATION KIT