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

Pulpdent Solo Flowable Composite with MCP

K Number: K153249 · Decision Apr 1, 2016
Classifications
1
FEI Numbers
204
Registration Numbers
204
Same Product Code
931
Applicant Total
32
Review Days
144

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
Pulpdent Solo Flowable Composite with MCP
K Number
K153249
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3690
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Pulpdent Corporation
Date Received
November 9, 2015
Decision Date
April 1, 2016
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

Similar 510(k) Clearances

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

View all

Other Clearances by Pulpdent Corporation

K Number Device Name
K210045 ACTIVA PRESTO PACK
K173020 OBA-MCP, Orthodontic Bracket Adhesive with MCP
K172169 Pulpdent (Activa) Pit and Fissure Sealant with MCP
K130223 RMGI FILL
K123265 RMGI LOW VISCOSITY
K120784 TUFF-TEMP 2.0
K120003 NUCAL
K120213 ETCH-RITE SUPREME
K113818 EMBRACE WETBOND PIT AND FISSURE SEALANT, LOW FILL
K113711 LIME-LITE II
Search all 32 clearances from Pulpdent Corporation →