Tulsa Dental Products, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tulsa Dental Products, Ltd. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Tulsa Dental Products, Ltd. has 8 FDA 510(k) cleared medical devices. Based in Tulsa, US.
Historical record: 8 cleared submissions from 1988 to 1997. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Tulsa Dental Products, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tulsa Dental Products, Ltd.
8 devices
Cleared
Mar 21, 1997
THERMAPREP PLUS OVEN
Dental
65d
Cleared
Feb 10, 1997
MINERAL TRIOXIDE AGGREGATE (MTA)
Dental
115d
Cleared
Jan 16, 1996
PROFILE NICKEL TITANIUM ROTARY INSTRUMENTS
Dental
89d
Cleared
May 26, 1994
THERMAPOST ENDODONTIC ROOT CANAL POST
Dental
708d
Cleared
Oct 20, 1993
PROFILE SERIES 29 FILES
Dental
89d
Cleared
Mar 29, 1991
THERMAPREP
Dental
70d
Cleared
Nov 13, 1990
THERMAFIL ENDODONTIC OBTURATOR
Dental
257d
Cleared
Apr 07, 1988
THERMAFIL ENDODONTIC OBTURATOR
Dental
21d