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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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Bio2 Technologies - B01010000711

VITRIUM C SMALL, 6 x 20
BIO2 TECHNOLOGIES, INC.
1000071
In Commercial Distribution

  • B01010000711 ()


  • Synthetic bone graft

Bio2 Technologies - B01010000701

VITRIUM C SMALL, 5 x 20
BIO2 TECHNOLOGIES, INC.
1000070
In Commercial Distribution

  • B01010000701 ()


  • Synthetic bone graft

Bio2 Technologies - B01010000691

VITRIUM C SMALL, 4 x 20
BIO2 TECHNOLOGIES, INC.
1000069
In Commercial Distribution

  • B01010000691 ()


  • Synthetic bone graft

Bio2 Technologies - B01010000601

VITRIUM C MEDIUM, 7 x 20
BIO2 TECHNOLOGIES, INC.
1000060
In Commercial Distribution

  • B01010000601 ()


  • Synthetic bone graft

Bio2 Technologies - B01010000591

VITRIUM C MEDIUM, 6 x 20
BIO2 TECHNOLOGIES, INC.
1000059
In Commercial Distribution

  • B01010000591 ()


  • Synthetic bone graft

Bio2 Technologies - B01010000581

VITRIUM C MEDIUM, 5 x 20
BIO2 TECHNOLOGIES, INC.
1000058
In Commercial Distribution

  • B01010000581 ()


  • Synthetic bone graft

Bio2 Technologies - B01010000571

VITRIUM C MEDIUM, 4 x 20
BIO2 TECHNOLOGIES, INC.
1000057
In Commercial Distribution

  • B01010000571 ()


  • Synthetic bone graft

Bausch + Lomb - 20757770469974

MILL LASER ENDO PROBE 20 ILLUM
Bausch & Lomb Incorporated
CX5984
In Commercial Distribution

  • 20757770469974 ()
  • 00757770469970 ()
CX5984

  • Phacoemulsification/vitrectomy system

Bausch + Lomb - 20757770059700

20 ga Combined Wide-Field Elite Pack
Bausch & Lomb Incorporated
SE5520W
In Commercial Distribution

  • 20757770059700 ()
  • 00757770059706 ()
SE5520W

  • Ophthalmic surgical procedure kit, non-medicated, single-use

Delicot - 20749915001309

Delicot 20 mm x 60 mm
AMERICAN SURGICAL COMPANY, LLC
63-09
In Commercial Distribution

  • 20749915001309 ()
  • 10749915001302 ()


  • Neurosurgical sponge
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