Aalba Dent, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aalba Dent, Inc. - FDA 510(k) Cleared Devices
27
Total
27
Cleared
0
Denied
Aalba Dent, Inc. has 27 FDA 510(k) cleared dental devices. Based in Chicago, US.
Historical record: 27 cleared submissions from 1985 to 2004.
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 - Aalba Dent, Inc.
27 devices
Cleared
Mar 04, 2004
CONTINUM V
Dental
37d
Cleared
Mar 03, 2004
CONTINUM
Dental
36d
Cleared
Dec 30, 2003
VERASOFT ES
Dental
101d
Cleared
Jul 22, 1998
VERABOND 2
Dental
37d
Cleared
Jan 05, 1998
NPG + 2
Dental
147d
Cleared
Oct 16, 1997
VERABOND 2V
Dental
48d
Cleared
Oct 10, 1997
PLATALLOY
Dental
91d
Cleared
Sep 05, 1997
VERA SOLDER
Dental
60d
Cleared
Sep 05, 1997
ALFALLOY
Dental
60d
Cleared
Aug 15, 1997
VERA PDN
Dental
71d
Cleared
Aug 15, 1997
AALBA GOLD SOLDER
Dental
39d
Cleared
Aug 15, 1997
VERA PD SOLDER
Dental
32d