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

LEXATITE QUICK ACRYLIC

K Number: K033432 · Decision Jan 15, 2004
Classifications
1
FEI Numbers
180
Registration Numbers
180
Same Product Code
188
Applicant Total
28
Review Days
79

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Basic Information

Device Name
LEXATITE QUICK ACRYLIC
K Number
K033432
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3770
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Imtec Corp.
Date Received
October 28, 2003
Decision Date
January 15, 2004
Product Code
EBG
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
EBG Crown And Bridge, Temporary, Resin

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Other Clearances by Imtec Corp.

K Number Device Name
K081653 MDI MII ONE-PIECE IMPLANT, 2.9MM
K081347 ILUMA VISION
K072660 ENDURE IMPLANT, MODEL 5108, 5111, 5113, 5114
K053046 ILUMA ORTHOCAT/DENTALCAT
K043226 ENDURE IMPLANT, MODELS 3508, 4308, 3520, 4320
K042289 MDI ORTHO
K031106 IMTEC SENDAX MDI AND MDI PLUS ENDOSSEOUS IMPLANT, MODELS OB-XX, SH-XX, MOB-22, MSH-XX
K030243 ENDURE IMPLANT, MODEL 3508,3511,3514,4308,4311,4314
K024044 SABER TECH IMPLANTS SYSTEM
K023067 IMTEC SENDAX MDI ORTHO6 AND ORTHO8
Search all 28 clearances from Imtec Corp. →