Scican , Ltd. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Scican , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: STATIM 6000B Vacuum Autoclave, Bravo G4 Chamber Autoclave, STATClave G4 Chamber Autoclave
11
Total
11
Cleared
0
Denied
Scican , Ltd. has 11 FDA 510(k) cleared general hospital devices. Based in Toronto, CA.
Last cleared in 2022. Active since 2007.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Scican , Ltd.
11 devices
Cleared
Mar 31, 2022
STATIM 6000B Vacuum Autoclave
General Hospital
94d
Cleared
Jul 01, 2021
Bravo G4 Chamber Autoclave
General Hospital
147d
Cleared
Jun 19, 2020
STATClave G4 Chamber Autoclave
General Hospital
248d
Cleared
Jul 26, 2019
STATCLAVE G4 Chamber Autoclave
General Hospital
192d
Cleared
Nov 24, 2017
SALUS - Hygiene Instrument Reprocessing Container
General Hospital
116d
Cleared
Jul 10, 2012
STATIM 2000 G4 CASSETTE
General Hospital
284d
Cleared
Jul 24, 2009
E-STATIS 40 SYSTEM
Dental
112d
Cleared
May 15, 2009
BRAVO AUTOCLAVE, MODELS 17, 17V AND 21V
General Hospital
101d
Cleared
Feb 04, 2008
STATMATIC 31 HANDPIECE MAINTENANCE UNIT
Dental
70d
Cleared
Dec 19, 2007
STATIM 7000 (WITHOUT USB PORT), MODEL 01-702100, STATIM 7000 (WITH USB PORT),...
General Hospital
106d
Cleared
Sep 13, 2007
STATIS DENTAL HANDPIECES
Dental
66d