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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 Type Device Class Implantable

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Allacor P - 00850039927362

Allacor P is derived from human umbilical cord extracellular matrix (ECM) and is indicated for the management of a range of acute and chronic wounds. As a resorbable particulate device, Allacor P is lyophilized and packaged in a sterile vial, allowing the device to be rehydrated and applied directly to the wound.
Stimlabs LLC
4 cc
In Commercial Distribution

  • 00850039927362 ()
AP-0040

  • Animal-derived wound matrix dressing

Allacor P - 00850039927355

Allacor P is derived from human umbilical cord extracellular matrix (ECM) and is indicated for the management of a range of acute and chronic wounds. As a resorbable particulate device, Allacor P is lyophilized and packaged in a sterile vial, allowing the device to be rehydrated and applied directly to the wound.
Stimlabs LLC
2 cc
In Commercial Distribution

  • 00850039927355 ()
AP-0020

  • Animal-derived wound matrix dressing

Allacor P - 00850039927348

Allacor P is derived from human umbilical cord extracellular matrix (ECM) and is indicated for the management of a range of acute and chronic wounds. As a resorbable particulate device, Allacor P is lyophilized and packaged in a sterile vial, allowing the device to be rehydrated and applied directly to the wound.
Stimlabs LLC
1 cc
In Commercial Distribution

  • 00850039927348 ()
AP-0010

  • Animal-derived wound matrix dressing

Corplex P - 00860471002572

Corplex P is derived from human umbilical cord extracellular matrix (ECM) and is indicated for the management of a range of acute and chronic wounds. As a resorbable particulate device, Corplex P/Theracor P/Allacor P is lyophilized and packaged in a sterile vial, allowing the device to be rehydrated and applied directly to the wound.
Stimlabs LLC
4 cc
In Commercial Distribution

  • 00860471002572 ()
CP-0040

  • Animal-derived wound matrix dressing

Corplex P - 00860471002565

Corplex P is derived from human umbilical cord extracellular matrix (ECM) and is indicated for the management of a range of acute and chronic wounds. As a resorbable particulate device, Corplex P/Theracor P/Allacor P is lyophilized and packaged in a sterile vial, allowing the device to be rehydrated and applied directly to the wound.
Stimlabs LLC
2 cc
In Commercial Distribution

  • 00860471002565 ()
CP0020

  • Animal-derived wound matrix dressing

Corplex P - 00860471002558

Corplex P is derived from human umbilical cord extracellular matrix (ECM) and is indicated for the management of a range of acute and chronic wounds. As a resorbable particulate device, Corplex P is lyophilized and packaged in a sterile vial, allowing the device to be rehydrated and applied directly to the wound.
Stimlabs LLC
1 cc
In Commercial Distribution

  • 00860471002558 ()
CP-0010

  • Animal-derived wound matrix dressing

Natrelle® Style 133 Tissue Expanders - 10888628004214

NATRELLE 133MX-16, 850 cc
Allergan, Inc.
133MX-16
Not in Commercial Distribution

  • 10888628004214 ()

  • 850 cc
133MX-16

  • Skin-port tissue expander

Natrelle® Style 133 Tissue Expanders - 10888628004207

NATRELLE 133MX-15, 700 cc
Allergan, Inc.
133MX-15
Not in Commercial Distribution

  • 10888628004207 ()

  • 700 cc
133MX-15

  • Skin-port tissue expander

Natrelle® Style 133 Tissue Expanders - 10888628004191

NATRELLE 133MX-14, 600 cc
Allergan, Inc.
133MX-14
Not in Commercial Distribution

  • 10888628004191 ()

  • 600 cc
133MX-14

  • Skin-port tissue expander

Natrelle® Style 133 Tissue Expanders - 10888628004184

NATRELLE 133MX-13, 500 cc
Allergan, Inc.
133MX-13
Not in Commercial Distribution

  • 10888628004184 ()

  • 500 cc
133MX-13

  • Skin-port tissue expander
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