Tulsa Dental Products, Ltd.

FDA Regulatory Profile

Tulsa Dental Products, Ltd. appears in FDA public data with 0 recalls, 8 510(k) clearances, 4 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 21, 1997.

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
4
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K970134THERMAPREP PLUS OVENMarch 21, 1997
K964174MINERAL TRIOXIDE AGGREGATE (MTA)February 10, 1997
K954790PROFILE NICKEL TITANIUM ROTARY INSTRUMENTSJanuary 16, 1996
K922931THERMAPOST ENDODONTIC ROOT CANAL POSTMay 26, 1994
K933582PROFILE SERIES 29 FILESOctober 20, 1993
K910224THERMAPREPMarch 29, 1991
K900986THERMAFIL ENDODONTIC OBTURATORNovember 13, 1990
K881139THERMAFIL ENDODONTIC OBTURATORApril 7, 1988