Medical Device Manufacturer · US , Mchenry , IL

Synthes (Usa) - FDA 510(k) Cleared Devices

411 submissions · 394 cleared · Since 1977

411

Total

394

Cleared

0

Denied

FDA 510(k) Regulatory Record - Synthes (Usa) Dental ✕

71 devices

1-12 of 71

Cleared Dec 20, 2010

SYNTHES DENTOALVEOLAR BONE FIXATION SYSTEM

Cleared Dec 16, 2010

SYNTHES ORTHODONTIC BONE ANCHOR SYSTEM

Cleared Jan 25, 2010

RAPIDSORB PLUS SCREW SYSTEM

Cleared Dec 11, 2009

SYNTHES MATRIXMANDIBLE SUBCONDYLAR PLATES

Cleared Aug 25, 2009

SYNTHES MATRIXMANDIBLE PREFORMED RECONSTRUCTION PLATES

Cleared Apr 30, 2009

SYNTHES 90 DEGREE SCREWDRIVER

Cleared Mar 12, 2009

SYNTHES MATRIXORTHOGNATHIS FIXATION SYSTEM

Cleared Nov 10, 2008

SYNTHES MATRIXMANDIBLE PLATE AND SCREW SYSTEM

Cleared Sep 05, 2008

MODIFICATION TO SYNTHES (USA) CONDYLAR HEAD ADD-ON SYSTEM

Cleared May 14, 2008

SYNTHES (USA) CURVILINEAR DISTRACTION SYSTEM

Cleared Apr 30, 2008

SYNTHES CRANIOFACIAL PLATE AND SCREW SYSTEM

Cleared Apr 16, 2007

THE SYNTHES MATRIXMANDIBLE PLATE AND SCREW SYSTEM

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