Novamin Technology, Inc. is one of 21641 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Novamin Technology, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ORALIEF OTC TOOTHPASTE FOR SENSITIVE TEETH, PERIOSRP TOOTH ROOT CONDITIONER WITH NOVAMIN, DENSHIELD TREATMENT FOR SENSITIVE TEETH
7
Total
7
Cleared
0
Denied
Novamin Technology, Inc. has 7 FDA 510(k) cleared medical devices. Based in Alachua, US.
Historical record: 7 cleared submissions from 2003 to 2008. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Novamin Technology, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by N.V. Kema as regulatory consultant.
FDA 510(k) Regulatory Record - Novamin Technology, Inc.
7 devices
Cleared
Mar 27, 2008
ORALIEF OTC TOOTHPASTE FOR SENSITIVE TEETH
Dental
57d
Cleared
May 18, 2007
PERIOSRP TOOTH ROOT CONDITIONER WITH NOVAMIN
Dental
11d
Cleared
Oct 18, 2006
DENSHIELD TREATMENT FOR SENSITIVE TEETH
Dental
155d
Cleared
Sep 02, 2004
ORALIEF THERAPY FOR SENSITIVE TEETH
Dental
153d
Cleared
Aug 23, 2004
BUTLER NUCARE PROPHYLAXIS PASTE WITH NOVAMIN
Dental
91d
Cleared
Mar 10, 2004
ORAVIVE TOOTH REVITALIZING PASTE
Dental
15d
Cleared
Oct 28, 2003
BUTLER NUCARE ROOT CONDITIONER WITH NOVAMIN
Dental
14d