Exmoor Plastics , Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
43
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K093863EPIDRUMMay 10, 2010
K990366EXMOOR SUCTION CLEARANCE KITMarch 5, 1999
K980828EXMOOR MYRINGOTOMY KITOctober 22, 1998
K981143DILKES LASER/SUCTION CANNULAESeptember 14, 1998
K972700EXMOOR ATTIC AND MASTOID ANTRUM MIDDLE EAR IMPLANT (EMMETT CAMPBELL MD FACS PATTERN)July 16, 1998
K981088MILLS COLUMELLA PROSTHESISJune 5, 1998
K981045EXMOOR TEFLON LOOP REPLACEMENT PROSTHESISMay 20, 1998
K974008PFLEIDERER'S INTRATYMPANIC CATHETERMay 13, 1998
K974224ENDOLYMPHATIC SAC TO MASTOID T-SHUNTJanuary 27, 1998
K973587EXMOOR TYMPANOCENTESIS KIT (TK/1)January 23, 1998
K974365MILLS INCUS HA SLEEVEJanuary 22, 1998
K974007SHAH PERMAVENTDecember 12, 1997
K963899CAUSSE UNIVERSAL OSSICULAR REPLACEMENT PROSTHESIS (ORP/1)August 22, 1997
K942745EXMOOR SINGLE USE MYRINGOTOMESSeptember 2, 1994
K942746SUCKER ENDS (ZOELLNER)August 24, 1994
K926462BEL-AIR VENTILATION TUBEMay 5, 1993
K921923TITANIUM VENTILATION TUBESFebruary 12, 1993
K924901DEANS DISPOSABLE T-TUBE INSERTERJanuary 28, 1993
K912486SINGH SPEECH SYSTEM (SERIES 'SSS')September 4, 1992
K911503EXMOOR SILICONE RUBBER SHEETNovember 19, 1991