Tuttnauer U.S.A Co, Ltd. is one of 16321 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tuttnauer U.S.A Co, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: T-Top 10 & T-Top T-Top 11, Pre-vacuum Tabletop Autoclave, TUTTNAUER ELARA-11 PRE-VACUUM TABLETOP AUTOCLAVE
9
Total
9
Cleared
0
Denied
Tuttnauer U.S.A Co, Ltd. has 9 FDA 510(k) cleared medical devices. Based in Washington, US.
Last cleared in 2023. Active since 1997. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Tuttnauer U.S.A Co, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Buchanan Ingersoll & Rooney PC as regulatory consultant.
FDA 510(k) Regulatory Record - Tuttnauer U.S.A Co, Ltd.
9 devices
Cleared
Nov 27, 2023
T-Top 10 & T-Top T-Top 11
General Hospital
88d
Cleared
Jan 15, 2015
Pre-vacuum Tabletop Autoclave
General Hospital
58d
Cleared
Aug 20, 2009
TUTTNAUER ELARA-11 PRE-VACUUM TABLETOP AUTOCLAVE
General Hospital
150d
Cleared
Aug 12, 2004
PRE-VACUUM AUTOCLAVE WITH STEAM GENERATOR AND VERTICAL SLIDING DOOR, MODELS...
General Hospital
392d
Cleared
Jul 25, 2002
TUTTNAUER EHS SERIES TABLE-TOP AUTOCLAVE, MODEL 2540
General Hospital
77d
Cleared
Feb 09, 2001
TUTTNAUER ELECTRONIC AUTOCLAVE, MODELS E, EA, EK, EKA, EP
General Hospital
452d
Cleared
Jul 09, 1999
TUTTNAUER MINI CONTAINER CASSETTE, TUTTNAUER STANDARD CASE CASSETTE
General Hospital
123d
Cleared
Nov 12, 1997
TUTTNAUER PREVACUUM TABLE AUTOCLAVE
General Hospital
518d
Cleared
Oct 29, 1997
TUTTNAUER TABLE-TOP AUTOCLAVE
General Hospital
41d