Austenal Dental, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Austenal Dental, Inc. - FDA 510(k) Cleared Devices
19
Total
19
Cleared
0
Denied
Austenal Dental, Inc. has 19 FDA 510(k) cleared dental devices. Based in Chicago, US.
Historical record: 19 cleared submissions from 1985 to 1989.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Austenal Dental, Inc.
19 devices
Cleared
Jul 14, 1989
OVERDENTURE - STUD ATTACHMENT
Dental
151d
Cleared
Oct 20, 1988
BASE, DENTURE, RELINING, REPAIRING, REBASING,RESIN
Dental
43d
Cleared
Apr 07, 1988
VITALLIUM EQUIPOISE ALLOY
Dental
37d
Cleared
Aug 10, 1987
LIGHT CURE DENTURE GLAZE
Dental
90d
Cleared
Jul 21, 1987
VITALLIUM WIRE
Dental
8d
Cleared
Mar 11, 1987
AUSTENAL ACUPAC 20 DENTURE BASE MATERIAL
Dental
175d
Cleared
Feb 19, 1987
AUSTENAL ACUSOFT SOFT LINER
Dental
231d
Cleared
Feb 19, 1987
AUSTENAL CONDENSING INSTRUMENT
Dental
58d
Cleared
Feb 10, 1987
A-SP ALLOY (SILVER-PALLADIUM CROWN & BRIDGE ALLOY)
Dental
63d
Cleared
Aug 26, 1986
PALLADIUM BASED DENT ALLOYS/PORCELAIN METAL RESTOR
Dental
28d
Cleared
Jul 31, 1986
COBALT, 29.5% CHROMIUM ALLOY DENTAL BAKE-ON ALLOY
Dental
17d
Cleared
Jul 18, 1986
AUSTENAL ACUPAC HI DENTURE BASE MATERIAL
Dental
15d