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

NEW STETIC ACRYLICS

K Number: K102874 · Decision Mar 28, 2011
Classifications
1
FEI Numbers
166
Registration Numbers
166
Same Product Code
329
Applicant Total
3
Review Days
179

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Basic Information

Device Name
NEW STETIC ACRYLICS
K Number
K102874
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3760
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
New Stetic
Date Received
September 30, 2010
Decision Date
March 28, 2011
Product Code
EBI
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
EBI Resin, Denture, Relining, Repairing, Rebasing

Similar 510(k) Clearances

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

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Other Clearances by New Stetic

K Number Device Name
K140125 NEW STETIC DENTAL AMALGAM ALLOY
K122925 NEW STETIC ARTIFICIAL TEETH