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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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Dental Implant Abutment
Ossvis Co., Ltd.
LWHA553
In Commercial Distribution

  • 08809918204195 ()


  • Dental implant suprastructure, temporary, preformed, single-use
Dental Implant Abutment
Ossvis Co., Ltd.
LWCS3520
In Commercial Distribution

  • 08809918204188 ()


  • Dental implant suprastructure, temporary, preformed, single-use
Dental Implant Abutment
Ossvis Co., Ltd.
LWCS3514
In Commercial Distribution

  • 08809918204171 ()


  • Dental implant suprastructure, temporary, preformed, single-use
Dental Implant Abutment
Ossvis Co., Ltd.
LWCS3504
In Commercial Distribution

  • 08809918204164 ()


  • Dental implant suprastructure, temporary, preformed, single-use
Dental Implant Abutment
Ossvis Co., Ltd.
LWHA607
In Commercial Distribution

  • 08809918203501 ()


  • Dental implant suprastructure, temporary, preformed, single-use
Dental Implant Abutment
Ossvis Co., Ltd.
LWHA606
In Commercial Distribution

  • 08809918203495 ()


  • Dental implant suprastructure, temporary, preformed, single-use
Dental Implant Abutment
Ossvis Co., Ltd.
LWHA605
In Commercial Distribution

  • 08809918203488 ()


  • Dental implant suprastructure, temporary, preformed, single-use
Dental Implant Abutment
Ossvis Co., Ltd.
LWHA604
In Commercial Distribution

  • 08809918203471 ()


  • Dental implant suprastructure, temporary, preformed, single-use
Dental Implant Abutment
Ossvis Co., Ltd.
LWHA603
In Commercial Distribution

  • 08809918203464 ()


  • Dental implant suprastructure, temporary, preformed, single-use
Dental Implant Abutment
Ossvis Co., Ltd.
LWHA509
In Commercial Distribution

  • 08809918203457 ()


  • Dental implant suprastructure, temporary, preformed, single-use
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