ClearanceBrief
Company ยท US

Tulsa Dental Products, Ltd.

FDA 510(k) clearances and medical device recalls filed under this name, 1988 to 1997. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
EKMGutta-Percha4
DZADrill, Dental, Intraoral1
EKSFile, Pulp Canal, Endodontic1
ELRPost, Root Canal1
KIFResin, Root Canal Filling1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Mar 21, 1997K970134THERMAPREP PLUS OVEN
Tulsa Dental Products, Ltd.
EKM
Feb 10, 1997K964174MINERAL TRIOXIDE AGGREGATE (MTA)
Tulsa Dental Products, Ltd.
KIF
Jan 16, 1996K954790PROFILE NICKEL TITANIUM ROTARY INSTRUMENTS
Tulsa Dental Products, Ltd.
DZA
May 26, 1994K922931THERMAPOST ENDODONTIC ROOT CANAL POST
Tulsa Dental Products, Ltd.
ELR
Oct 20, 1993K933582PROFILE SERIES 29 FILES
Tulsa Dental Products, Ltd.
EKS
Mar 29, 1991K910224THERMAPREP
Tulsa Dental Products, Ltd.
EKM
Nov 13, 1990K900986THERMAFIL ENDODONTIC OBTURATOR
Tulsa Dental Products, Ltd.
EKM
Apr 7, 1988K881139THERMAFIL ENDODONTIC OBTURATOR
Tulsa Dental Products, Ltd.
EKM

Latest recalls

DateFirm and productCodeLinked 510(k)
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