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

P1145 Dental Restorative

K Number: K162257 · Decision Nov 7, 2016
Classifications
1
FEI Numbers
204
Registration Numbers
204
Same Product Code
931
Applicant Total
32
Review Days
88

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
P1145 Dental Restorative
K Number
K162257
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3690
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kerr Corporation
Date Received
August 11, 2016
Decision Date
November 7, 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 Kerr Corporation

K Number Device Name
K252890 ZenSeal Pro
K222830 Rainbow 360
K221255 SimpliShade Bulk Fill, SimpliShade Bulk Fill Flow
K191548 Nexus Universal Self-Cure
K182162 OptiBond eXTRa Universal
K162948 Styptin, Hemogin-L, Hemodettes, and GingiGEL Aluminum Chloride Impregnated Retraction Cord/Materials
K163064 Demi Ultra
K162536 GingiKnit+, GingiBraid+, GingiBraid+ Shortcut, and UniBraid+ impregnated Aluminum Potassium Sulfate Retraction Cord
K162164 GingiKnit+, GingiBraid+, and Shortcut with GingiBraid+ Non-Impregnated Retraction Cord
K162436 EndoVac Pure
Search all 32 clearances from Kerr Corporation →