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

OVERDENTURE - STUD ATTACHMENT

K Number: K890713 · Decision Jul 14, 1989
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
19
Review Days
151

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Basic Information

Device Name
OVERDENTURE - STUD ATTACHMENT
K Number
K890713
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Austenal Dental, Inc.
Date Received
February 13, 1989
Decision Date
July 14, 1989
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

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Other Clearances by Austenal Dental, Inc.

K Number Device Name
K883799 BASE, DENTURE, RELINING, REPAIRING, REBASING,RESIN
K880875 VITALLIUM EQUIPOISE ALLOY
K871849 LIGHT CURE DENTURE GLAZE
K872746 VITALLIUM WIRE
K863630 AUSTENAL ACUPAC 20 DENTURE BASE MATERIAL
K862557 AUSTENAL ACUSOFT SOFT LINER
K865025 AUSTENAL CONDENSING INSTRUMENT
K864826 A-SP ALLOY (SILVER-PALLADIUM CROWN & BRIDGE ALLOY)
K862856 PALLADIUM BASED DENT ALLOYS/PORCELAIN METAL RESTOR
K862667 COBALT, 29.5% CHROMIUM ALLOY DENTAL BAKE-ON ALLOY
Search all 19 clearances from Austenal Dental, Inc. →