FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

X-SMART EASY

K Number: K092614 · Decision Dec 2, 2009
Classifications
1
FEI Numbers
88
Registration Numbers
88
Same Product Code
88
Applicant Total
13
Review Days
98

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Basic Information

Device Name
X-SMART EASY
K Number
K092614
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.4200
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dentsply Interntional
Date Received
August 26, 2009
Decision Date
December 2, 2009
Product Code
EKX
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
EKX Handpiece, Direct Drive, Ac-Powered

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Other Clearances by Dentsply Interntional

K Number Device Name
K092030 ELATION MB METAL REINFORCED PLASTIC BRACKET
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K082973 STER-MATE STERILE LAVAGE KIT
K082974 MYSTIQUE MB CERAMIC BRACKETS
K081291 PRE-CEMENTED ORTHODONTIC BRACKET SYSTEM EXTENSION
K080311 MODIFIED TEMPRX ESTHETIC PROVISIONAL SYSTEM
K080246 COMPOSITE ALIGNER BUTTON
K080203 MTA ROOT CANAL SEALER
K073173 SELF-ADHESIVE RESIN CEMENT
K073218 MTA ADVANCED MATERIAL
Search all 13 clearances from Dentsply Interntional →