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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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ACRYSOF® ACRYSERT® - 00380652249294

AcrySof(R) IQ ASPHERIC IOL, SP ACRYLIC FOLDABLELENS, w/AcrySert(R) DELIVERY SYSTEM, UV w/BLUELIGHT FILTER, 13.0mm LENGTH, 6.0mm ANTERIORASYMMETRIC BICONVEX OPTIC, PLANAR HAPTICS.
Alcon Laboratories, Inc.
SN6CWS
Not in Commercial Distribution

  • 00380652249294 ()

  • Diopter 24
SN6CWS.240

  • Posterior-chamber intraocular lens, pseudophakic

ACRYSOF® IQ RESTOR® - 00380652241762

AcrySof(R) IQ ReSTOR(R) MULTIFOCAL IOL, SINGLE-PIECE ACRYLIC FOLDABLE LENS, UV WITH BLUE LIGHTFILTER, 13.0mm LENGTH, 6.0mm APODIZEDDIFFRACTIVE ASPHERIC OPTIC.
Alcon Laboratories, Inc.
SN6AD1
Not in Commercial Distribution

  • 00380652241762 ()

  • Diopter 24


  • Posterior-chamber intraocular lens, pseudophakic

ACRYSOF® IQ RESTOR® - 00380652241311

AcrySof(R) IQ ReSTOR(R) MULTIFOCAL IOL, SINGLE-PIECE ACRYLIC FOLDABLE LENS, UV WITH BLUE LIGHTFILTER, 13.0mm LENGTH, 6.0mm APODIZEDDIFFRACTIVE ASPHERIC OPTIC.
Alcon Laboratories, Inc.
SN6AD1
Not in Commercial Distribution

  • 00380652241311 ()

  • Diopter 24


  • Posterior-chamber intraocular lens, pseudophakic

ACRYSOF ULTRASERT - 00380652358354

AcrySof(R) IQ ASPHERIC IOL SP ACRYLIC FOLDABLELENS wUltraSert(TM) DELIVERY SYSTEM UV wBLUE LIGHT FILTER. 13.0mm LENGTH 6.0mm ANTERIORASYMMETRIC BICONVEX OPTIC PLANAR HAPTICS.
Alcon Laboratories, Inc.
AU00T0
In Commercial Distribution

  • 00380652358354 ()

  • Diopter 24
AU00T0.240

  • Posterior-chamber intraocular lens, pseudophakic

ACRYSOF® - 00380652332743

AcrySof(R) ASPHERIC IOL, SINGLE-PIECE ACRYLICFOLDABLE POSTERIOR CHAMBER LENS,UV-ABSORBING, 13.0mm LENGTH, 6.0mm ANTERIORASYMMETRIC BICONVEX OPTIC, PLANAR HAPTICS.
Alcon Laboratories, Inc.
SA60WF
In Commercial Distribution

  • 00380652332743 ()

  • Diopter 24
SA60WF.240

  • Posterior-chamber intraocular lens, pseudophakic

Wagner SL Revision® - 00889024480636

No Description
Zimmer GmbH
01.00103.024
In Commercial Distribution

  • 00889024480636 ()

  • 24 305mm
01.00103.024

  • Revision uncoated hip femur prosthesis

Wagner SL Revision® - 00889024593534

No Description
Zimmer GmbH
01.00102.624
In Commercial Distribution

  • 00889024593534 ()

  • 24 265mm
01.00102.624

  • Revision uncoated hip femur prosthesis

DISTRACTION, INTERNAL - 00888118080790

TUBE, LEFORT 1, ADJ MIDFACE, BUTTRESS, ADJ LENGTH, TI-6AL-4V
KLS-Martin L.P.
51-402-24-09
Not in Commercial Distribution

  • 00888118080790 ()

  • 24 MM


  • Implantable craniofacial bone distractor

DISTRACTION, INTERNAL, STERILE - 00888118104564

TUBE, LEFORT 1, ADJ MIDFACE, BUTTRESS, ADJ LENGTH, TI-6AL-4V
KLS-Martin L.P.
51-402-24-71
Not in Commercial Distribution

  • 00888118104564 ()

  • 24 MM


  • Implantable craniofacial bone distractor

RINGLOC® HIP SYSTEM - 00887868230028

No Description
Biomet Orthopedics, LLC
105424
In Commercial Distribution

  • 00887868230028 ()

  • 24 SIZE
105424

  • Acetabular shell
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