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

SPI DENTAL IMPLANT INICELL

K Number: K090154 · Decision Jul 27, 2009
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
26
Review Days
186

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Basic Information

Device Name
SPI DENTAL IMPLANT INICELL
K Number
K090154
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Thommen Medical AG
Date Received
January 22, 2009
Decision Date
July 27, 2009
Product Code
DZE
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
DZE Implant, Endosseous, Root-Form

Similar 510(k) Clearances

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Other Clearances by Thommen Medical AG

K Number Device Name
K171795 Thommen Implant System
K160244 VARIOunite
K151984 Thommen Milling Abutment for CAD/CAM
K121334 VARIOECO
K111984 SPI VARIO ANGLED ABUTMENT
K102804 SPI TITANIUM BASE FOR CAD/CAM
K101798 SPI VARIOMULTI ANGLED ABUTMENT
K093615 SPI DENTAL IMPLANT, ELEMENT
K092248 SPI CUSTOMIZABLE GINGIVA FORMER
K090153 SPI VARIOMULTI ANGLED ABUTMENT
Search all 26 clearances from Thommen Medical AG →