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FDA 510(k) Applications Submitted by STEVE RUDOLPH
FDA 510(k) Number
Submission Date
Device Name
Applicant
K040343
02/12/2004
TEMP F
NOVOCOL, INC.
K120619
02/29/2012
ORTHODONTIC FLOWABLE BRACKET ADHESIVE
NOVOCOL, INC.
K101540
06/03/2010
GRANITEC DUAL-CURE CORE BUILD-UP, N'DURANCE DIMER CORE
NOVOCOL INC. DBA SEPTODONT AND CONFI-DENTAL PRODUC
K072150
08/03/2007
DIMER ACID DERIVED NANO-HYBRID COMPOSITE RESTORATIVE MATERIAL
NOVOCOL, INC.
K092501
08/14/2009
LIGHT-ACTIVATED LOW-STRESS THIOL-ENE COMPOSITE RESTORATIVE MATERIAL
NOVOCOL, INC.
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