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

CHAIRSIDE ATTACHMENT PROCESSING MATERIAL

K Number: K140570 · Decision Jun 16, 2014
Classifications
1
FEI Numbers
166
Registration Numbers
166
Same Product Code
329
Applicant Total
12
Review Days
102

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Basic Information

Device Name
CHAIRSIDE ATTACHMENT PROCESSING MATERIAL
K Number
K140570
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3760
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Zest Anchors, LLC
Date Received
March 6, 2014
Decision Date
June 16, 2014
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

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Other Clearances by Zest Anchors, LLC

K Number Device Name
K260555 LOCATOR® Angled Abutment
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K250721 LOCATOR® Angled Abutment
K243272 LOCATOR Angled Abutment
K233587 LOCATOR Angled Abutment (Various)
K220252 High Retention Attachment System
K213391 High Retention Attachment System
K191619 TurboTemp EZ
K151789 LOCATOR F-Tx Attachment System
K133327 SATURNO(TM) OVERDENTURE IMPLANT SYSTEM
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