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Walter Lorenz Surgical, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
56
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K063386LORENZ ORTHODONTIC ANCHORAGE SYSTEMFebruary 9, 2007
K063052LORENZ TITANIUM FRACTURE / RECONSTRUCTION DEVICES AND PRE-BENT PLATESJanuary 12, 2007
K063506LORENZ STERNAL CLOSURE SYSTEMDecember 18, 2006
K062842TWIST DRILLDecember 4, 2006
K061384LORENZ PECTUS SUPPORT BAR, TITANIUM; LORENZ PECTUS SUPPORT BAR STABILIZER, TITANIUMJune 6, 2006
K042516OTOMIMIXNovember 8, 2004
K030425LORENZ RESORBABLE DISTRACTION SYSTEM OR EXPANDERMay 14, 2004
K040990MODIFICATION TO SELF-DRILLING RADIOGRAPHIC MARKERSMay 13, 2004
K040983LORENZ SELF-DRILLING IMF SCREWMay 5, 2004
K033740LORENZ STERNAL CLOSURE SYSTEMDecember 15, 2003
K032228LORENZ 2.4 SELF DRILLING SCREWSAugust 11, 2003
K031751RAPIDFIRE SELF DRILLING SCREWSJune 26, 2003
K031696LORENZE EXTERNAL MANDIBULAR DISTRACTORJune 17, 2003
K031034SPIN DOWN RAPIDFLAPMay 21, 2003
K023718QUICKSET MIMIX BONE VOID FILLERDecember 4, 2002
K021522LORENZ 1.5 X 4 MM LACTOSORB TAP FREE SCREWMay 21, 2002
K013954LORENZ SELF DRILLING SCREWSFebruary 28, 2002
K020407LORENZ BLUE DEVICEFebruary 22, 2002
K014148SELF-DRILLING RADIOGRAPHIC MARKERJanuary 17, 2002
K013557LACTOSORB CRANIOFACIAL ANCHOR-PUSH SCREWNovember 16, 2001