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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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Optium® - 00889858450560

Optium DBM Gel
LIFENET HEALTH
TGEL05
In Commercial Distribution

  • 00889858450560 ()

  • 5 cc
TGEL05

  • Bone matrix implant, human-derived

Optium® - 00889858450546

Optium DBM Gel
LIFENET HEALTH
TGEL01
In Commercial Distribution

  • 00889858450546 ()

  • 1 cc
TGEL01

  • Bone matrix implant, human-derived

VESUVIUS™ - 00889858002813

DBM Putty
LIFENET HEALTH
4104-K0100DP-01
In Commercial Distribution

  • 00889858002813 ()

  • 10 cc
4104-K0100DP

  • Bone matrix implant, human-derived

VESUVIUS™ - 00889858002790

DBM Putty
LIFENET HEALTH
4104-K0050DP-01
In Commercial Distribution

  • 00889858002790 ()

  • 5 cc
4104-K0050DP

  • Bone matrix implant, human-derived

VESUVIUS™ - 00889858002752

DBM Putty
LIFENET HEALTH
4104-K0025DP-01
In Commercial Distribution

  • 00889858002752 ()

  • 2.5 cc
4104-K0025DP

  • Bone matrix implant, human-derived

VESUVIUS™ - 00889858002714

DBM Putty
LIFENET HEALTH
4104-K0010DP-01
In Commercial Distribution

  • 00889858002714 ()

  • 1 cc
4104-K0010DP

  • Bone matrix implant, human-derived

Optetrak - 10885862053497

No Description
Exactech, Inc.
208-04-72
In Commercial Distribution

  • 10885862053497 ()

  • Size CC
208-04-72

  • Tibial insert

STIMUBLAST® - M536ABS2004081

STIMUBLAST® CB DBM Paste, 8cc
ALLOSOURCE
ABS-2004-08
In Commercial Distribution

  • M536ABS2004081 ()

  • 8 cc
ABS-2004-08

  • Bone matrix implant, human-derived

STIMUBLAST® - M536ABS2004031

STIMUBLAST® CB DBM Paste, 3cc
ALLOSOURCE
ABS-2004-03
In Commercial Distribution

  • M536ABS2004031 ()

  • 3 cc
ABS-2004-03

  • Bone matrix implant, human-derived

STIMUBLAST® - M536ABS2004011

STIMUBLAST® CB DBM Paste, 1cc
ALLOSOURCE
ABS-2004-01
In Commercial Distribution

  • M536ABS2004011 ()

  • 1 cc
ABS-2004-01

  • Bone matrix implant, human-derived
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