Innovative Bioceramix, Inc. is one of 507 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Innovative Bioceramix, Inc. - FDA 510(k) Cleared Devices
Recent clearances: iRoot SP Plus, iRoot BP Root Repair Material BioAggregate Paste, IROOT FM
8
Total
8
Cleared
0
Denied
Innovative Bioceramix, Inc. has 8 FDA 510(k) cleared medical devices. Based in Vancouver, Bc, CA.
Last cleared in 2023. Active since 2006. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Innovative Bioceramix, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Innovative Bioceramix, Inc.
8 devices
Cleared
May 31, 2023
iRoot SP Plus
Dental
30d
Cleared
Nov 22, 2022
iRoot BP Root Repair Material BioAggregate Paste
Dental
55d
Cleared
Sep 18, 2014
IROOT FM
Dental
588d
Cleared
Dec 03, 2010
IROOT FS
Dental
64d
Cleared
Sep 28, 2009
IROOT BP PLUS
Dental
25d
Cleared
Jan 06, 2009
IROOT BP, MODEL IRBP 4609
Dental
96d
Cleared
Apr 09, 2008
IROOT SP
Dental
8d
Cleared
Nov 21, 2006
BIOAGGREGATE
Dental
8d