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

BELLEGLAZE

K Number: K992067 · Decision Aug 27, 1999
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
50
Applicant Total
17
Review Days
70

Basic Information

Device Name
BELLEGLAZE
K Number
K992067
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3310
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
KERR DENTAL MATERIALS CENTER
Date Received
June 18, 1999
Decision Date
August 27, 1999
Product Code
EBD
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
EBD Coating, Filling Material, Resin

Similar 510(k) Clearances

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

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Other Clearances by KERR DENTAL MATERIALS CENTER

K Number Device Name
K050984 BIOPLANT
K031444 OPTIBOND FL
K030646 BELLEGLASS POINT 4
K020303 XR PRIMER 2
K020178 BELLEGLASS HP MODELING GEL
K020092 TEMPHASE
K014027 OPTIBOND SOLO PLUS 4
K013375 BELLEGLASS HP OPAQUE 2
K013325 POINT 4 FLOWABLE 2
K011908 OPTIBOND SOLO PLUS 3
Search all 17 clearances from KERR DENTAL MATERIALS CENTER →