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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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LAL, Sterile, Packaged, 26.0 Diopter
RXSIGHT, INC.
60005-3260
In Commercial Distribution

  • 00818806020777 ()


  • Posterior-chamber intraocular lens, pseudophakic
LAL, Sterile, Packaged, 25.0 Diopter
RXSIGHT, INC.
60005-3250
In Commercial Distribution

  • 00818806020760 ()


  • Posterior-chamber intraocular lens, pseudophakic
LAL, Sterile, Packaged, 24.0 Diopter
RXSIGHT, INC.
60005-3240
In Commercial Distribution

  • 00818806020753 ()


  • Posterior-chamber intraocular lens, pseudophakic
LAL, Sterile, Packaged, 23.5 Diopter
RXSIGHT, INC.
60005-3235
In Commercial Distribution

  • 00818806020746 ()


  • Posterior-chamber intraocular lens, pseudophakic
LAL, Sterile, Packaged, 23.0 Diopter
RXSIGHT, INC.
60005-3230
In Commercial Distribution

  • 00818806020739 ()


  • Posterior-chamber intraocular lens, pseudophakic
LAL, Sterile, Packaged, 22.5 Diopter
RXSIGHT, INC.
60005-3225
In Commercial Distribution

  • 00818806020722 ()


  • Posterior-chamber intraocular lens, pseudophakic
LAL, Sterile, Packaged, 22.0 Diopter
RXSIGHT, INC.
60005-3220
In Commercial Distribution

  • 00818806020715 ()


  • Posterior-chamber intraocular lens, pseudophakic
LAL, Sterile, Packaged, 21.5 Diopter
RXSIGHT, INC.
60005-3215
In Commercial Distribution

  • 00818806020708 ()


  • Posterior-chamber intraocular lens, pseudophakic
LAL, Sterile, Packaged, 21.0 Diopter
RXSIGHT, INC.
60005-3210
In Commercial Distribution

  • 00818806020692 ()


  • Posterior-chamber intraocular lens, pseudophakic
LAL, Sterile, Packaged, 20.5 Diopter
RXSIGHT, INC.
60005-3205
In Commercial Distribution

  • 00818806020685 ()


  • Posterior-chamber intraocular lens, pseudophakic
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