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

HyperFil-LV

K Number: K182296 · Decision Dec 14, 2018
Classifications
1
FEI Numbers
204
Registration Numbers
204
Same Product Code
931
Applicant Total
53
Review Days
112

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Basic Information

Device Name
HyperFil-LV
K Number
K182296
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3690
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Parkell, Inc.
Date Received
August 24, 2018
Decision Date
December 14, 2018
Product Code
EBF
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
EBF Material, Tooth Shade, Resin

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Other Clearances by Parkell, Inc.

K Number Device Name
K243254 Parkell Pit and Fissure Sealant
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K191103 Parkell Desensitizer Gel
K190930 SmarTemp X1
K172176 Parkell Universal Adhesive
K151518 BRUSH&BOND PLUS
K142848 EAZY PRIMER
K132115 ABSOLUTE DENTIN 2
K113839 RETRACT GINGIVAL RETRACTION/HEMOSTATIC PASTE
K101044 RETRIEVE IMPLANT CEMENT
Search all 53 clearances from Parkell, Inc. →