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

OptiBond eXTRa Universal

K Number: K182162 · Decision Nov 7, 2018
Classifications
1
FEI Numbers
137
Registration Numbers
137
Same Product Code
418
Applicant Total
32
Review Days
89

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
OptiBond eXTRa Universal
K Number
K182162
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3200
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kerr Corporation
Date Received
August 10, 2018
Decision Date
November 7, 2018
Product Code
KLE
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
KLE Agent, Tooth Bonding, Resin

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KLE), 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
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
K162257 P1145 Dental Restorative
Search all 32 clearances from Kerr Corporation →