OmniFit HFx Hip Stem

FDA registration

HOWMEDICA OSTEONICS CORP·3 products·🇺🇸 United States

Accolade HFX Femoral Stem

FDA registration

Polymer Corporation·3 products·🇺🇸 United States

INSTRUMENT

FDA UDI

Howmedica Osteonics Corp.·07613327240191·HFX STEM INSERTER

INSTRUMENT

FDA UDI

Howmedica Osteonics Corp.·07613327208788·OMNIFIT HFX BROACH PF5

INSTRUMENT

FDA UDI

Howmedica Osteonics Corp.·07613327252811·ACCOLADE HFX BROACH TRAY

INSTRUMENT

FDA UDI

Howmedica Osteonics Corp.·07613327208825·OMNIFIT HFX BROACH C5/PF7

INSTRUMENT

FDA UDI

Howmedica Osteonics Corp.·07613327208856·OMNIFIT HFX BROACH C10/PF12

INSTRUMENT

FDA UDI

Howmedica Osteonics Corp.·07613327208818·OMNIFIT HFX BROACH C11/PF13

INSTRUMENT

FDA UDI

Howmedica Osteonics Corp.·07613327208740·OMNIFIT HFX BROACH C4/PF6

INSTRUMENT

FDA UDI

Howmedica Osteonics Corp.·07613327208795·OMNIFIT HFX BROACH C7/PF9

INSTRUMENT

FDA UDI

Howmedica Osteonics Corp.·07613327208887·OMNIFIT HFX BROACH C6/PF8

Senza

FDA UDI

NEVRO CORP.·00813426020817·HFX iQ Patient Application (iOS)

INSTRUMENT

FDA UDI

Howmedica Osteonics Corp.·07613327208863·OMNIFIT HFX BROACH C8/PF10

INSTRUMENT

FDA UDI

Howmedica Osteonics Corp.·07613327208801·OMNIFIT HFX BROACH C9/PF11

ATHENA HFX

FDA 510(k)

FDA Class 2 ·Radiology

Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

FDA Pre-Market Approval

FDA Class 3 ·Senza HFX iQ System, Senza HFX iQ IPG, HFX Trial Stimulator, HFX iQ Remote, HFX iQ Patient Application

Circumcision Clamp

FDA registration

SONTEC INSTRUMENTS, INC.·1 product·🇺🇸 United States

KMEDIC

FDA registration

Teleflex LLC (NADC)·1 product·🇺🇸 United States

wee BELL Newborn Circumcision Device

FDA registration

POTTYMD, LLC·1 product·🇺🇸 United States

Sterigenics U.S., LLC

FDA registration

Sterigenics U.S., LLC·1 product·🇺🇸 United States