Aseptico, Inc. is one of 5098 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aseptico, Inc. - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
Aseptico, Inc. has 18 FDA 510(k) cleared dental devices. Based in Kirkland, US.
Historical record: 18 cleared submissions from 1988 to 2015.
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 - Aseptico, Inc.
18 devices
Cleared
May 28, 2015
AEU-7000L-70V IMPLANT/ENDODONTIC DENTAL SYSTEM (LIGHTED VERSION)
Dental
127d
Cleared
Dec 31, 2014
AEU-6000 IMPLANT / ENDODONTIC DENTAL SYSTEM
Dental
149d
Cleared
Aug 14, 2013
AEU-525 TRANSPORT III PORTABLE DENTAL SYSTEM
Dental
153d
Cleared
Jun 14, 2011
AEU-26L ELCTRONIC ENDODONTIC SYSTEM
Dental
57d
Cleared
Apr 11, 2011
AMC-20 PORTABLE DENTAL CART MODEL AMC-20
Dental
334d
Cleared
Feb 28, 2011
GENERAL DENISTRY MOTOR
Dental
101d
Cleared
Apr 11, 2007
ASC-12 PIEZOELECTRIC SCALER
Dental
13d
Cleared
May 03, 2005
E-TYPE STRAIGHT HANDPIECE, MODEL AHP-101
Dental
6d
Cleared
Mar 18, 2005
AEU-14CF EXPENDITION
Dental
49d
Cleared
Dec 03, 2003
ASEPTICO ENDOPEX V, MODEL AEU-40
Dental
257d
Cleared
Mar 03, 2003
ASEPTICO VCT VERSATILE COMMAND TECHNOLOGY MODEL AEU-925
Dental
46d
Cleared
Oct 24, 2002
AEU-425 TRANSPORT II PORTABLE DENTAL SYSTEM
Dental
108d