Sultan Chemists, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sultan Chemists, Inc. - FDA 510(k) Cleared Devices
11
Total
10
Cleared
0
Denied
Sultan Chemists, Inc. has 10 FDA 510(k) cleared medical devices. Based in Westford, US.
Historical record: 10 cleared submissions from 1990 to 2005. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Sultan Chemists, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sultan Chemists, Inc.
11 devices
Cleared
Nov 16, 2005
VERSA-LINK PORCELAIN BONDING SYSTEM
Dental
49d
Cleared
Oct 20, 2005
SILGIMIX ALGINATE REPLACEMENT IMPRESSION MATERIAL
Dental
49d
Cleared
Feb 18, 2005
GENIE MAGIC MIX ULTRA HYDROPHILIC IMPRESSION MATERIAL
Dental
105d
Cleared
Apr 09, 2003
GENIE ULTRA HYDROPHILIC IMPRESSION MATERIAL
Dental
61d
Cleared
May 07, 2002
SULTAN SPOROX TEST VIAL, MODEL 75195
General Hospital
71d
Cleared
Nov 15, 2000
SULTAN SENSITEMP RESIN TEMPORARY CEMENT, MODEL 70010
Dental
64d
Cleared
Jul 14, 1999
PRO-PORTION CLEANER/DISINFECTANT
General Hospital
75d
Cleared
Jul 21, 1997
DINABASE (TM)
Dental
115d
Cleared
May 17, 1995
ASSURE, SELF-SEALING STERILIZATION POUCH
General Hospital
41d
Cleared
Jun 21, 1994
ASSURE SELF SEALING STERILIZATION POUCH
General Hospital
323d
Cleared
Mar 02, 1990
SULTAN PERIO-SELECT IRRIGATION SYSTEM
Dental
88d