Bionix Development Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
12
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K153270TruGuard Custom Tongue and Jaw PositionerMarch 8, 2016
K123411LITTLE ANGELS SWADDLING BLANKETMarch 7, 2013
K120335EMBRACE THERMOPLASTICMay 3, 2012
K100691OMNI V SBRT POSITIONING SYSTEM, MODEL RT-4500May 11, 2010
K100264T-FORM EXTREMITY IMMOBILIZER, MODEL RT-6060April 9, 2010
K050701THIGH AND FOOT POSITIONER, SUPRONE PLUS, MODEL RT-6010April 1, 2005
K040773PELVIS BELLYBOARD PLUS PATIENT POSITIONING SYSTEMApril 9, 2004
K030051VERSABOARD, MODEL 7040April 4, 2003
K933614PITUITARY BOARDOctober 7, 1993
K9336133-WAY HEAD IMMOBILIZER; 3WAY DELUXE REUSABLE FRAME HEAD IMMOBILIZEROctober 7, 1993
K905007STANDARD BREAST BOARDS; DELUXE BREAST BOARDFebruary 12, 1991
K900370ONE/CIRC (CIRCUMCISION CLAMP)April 16, 1990