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AlloDermTM Regenerative Tissue Matrix (RTM)
portfolio of products

    AlloDerm™ RTM is:
  • Sterile
  • Ready-to-use with a minimum 2-minute soak
  • Able to be stored without refrigeration
  • Available in 5 thicknesses for implantable and graftable applications
  • Available in a variety of textures:
  • - Implantable: Perforated, Nonperforated
    -Graftable: Fenestrated, Meshed, Nonmeshed

With an extensive portfolio of shapes, sizes, and thicknesses, there’s an AlloDerm™ RTM product to meet the
needs of a range of patients and procedures. Plus, every piece is covered by the AlloDerm™ RTM Guarantee.

Select a shape and texture below to view the available sizes and thicknesses for order.

Implantable

Perforated

AlloDerm™ RTM Contour PerforatedAlloDerm™ RTM Contour PerforatedAlloDerm™ RTM Contour Perforated
AlloDerm™ RTM Perforated RectangleAlloDerm™ RTM Perforated RectangleAlloDerm™ RTM Perforated Rectangle

Nonperforated

AlloDerm™ RTM ContourAlloDerm™ RTM ContourAlloDerm™ RTM Contour
AlloDerm™ RTM Perforated RectangleAlloDerm™ RTM Perforated RectangleAlloDerm™ RTM Perforated Rectangle

Graftable

Fenestrated

Meshed

Nonmeshed

Contour Perforated sizes and thicknesses

AlloDerm SELECT™
Regenerative Tissue Matrix AlloDerm™ RTM Contour Perforated sizes and thicknesses Contour Perforated

Product Description Piece Size (cm) Coverage (cm2) Thickness Thickness Range (mm) Product Code
AlloDerm SELECT™ Regenerative Tissue Matrix AlloDerm™ RTM Contour Perforated sizes and thicknesses Contour Perforated X-Large
11.8 x 23.7
200 Medium 1.6 ± 0.4mm CXL1519P
Thick 2.4 ± 0.4mm CXL1518P
Large
10.7 x 21.5
164 Thin 1.0 ± 0.2mm CL1516P
Medium 1.6 ± 0.4mm CL1518P
Thick 2.4 ± 0.4mm CL1519P
Medium
9.6 x 19.3
132 Thin 1.0 ± 0.2mm CM1516P
Medium 1.6 ± 0.4mm CM1518P
Thick 2.4 ± 0.4mm CM1519P
Small
7.3 x 14.7
77 Thin 1.0 ± 0.2mm CS1516P
Medium 1.6 ± 0.4mm CS1518P
Thick 2.4 ± 0.4mm CS1519P

Contour sizes and thicknesses

AlloDerm SELECT™
Regenerative Tissue Matrix AlloDerm™ RTM Contour sizes and thicknesses Contour

Product Description Piece Size (cm) Coverage (cm2) Thickness Thickness Range (mm) Product Code
AlloDerm SELECT™ Regenerative Tissue Matrix AlloDerm™ RTM Contour sizes and thicknesses Contour X-Large
11.8 x 23.7
200 Medium 1.6 ± 0.4mm CXL1518
Thick 2.4 ± 0.4mm CXL1519
Large
10.7 x 21.5
164 Thin 1.0 ± 0.2mm CL1516
Medium 1.6 ± 0.4mm CL1518
Thick 2.4 ± 0.4mm CL1519
Medium
9.6 x 19.3
132 Thin 1.0 ± 0.2mm CM1516
Medium 1.6 ± 0.4mm CM1518
Thick 2.4 ± 0.4mm CM1519
Small
7.3 x 14.7
77 Thin 1.0 ± 0.2mm CS1516
Medium 1.6 ± 0.4mm CS1518
Thick 2.4 ± 0.4mm CS1519

Perforated Rectangle sizes and thicknesses

AlloDerm SELECT™
Regenerative Tissue Matrix AlloDerm™ RTM Perforated Rectangle sizes and thicknesses Perforated Rectangle

Product Description Piece Size (cm) Coverage (cm2) Thickness Thickness Range (mm) Product Code
AlloDerm SELECT™ Regenerative Tissue Matrix AlloDerm™ RTM Perforated Rectangle sizes and thicknesses Perforated Rectangle 16 x 20 320 Medium 1.6 ± 0.4mm 1518320P
Thick 2.4 ± 0.4mm 1519320P
X-Thick 3.4 ± 0.6mm 1522320P

Rectangle sizes and thicknesses

AlloDerm SELECT™
Regenerative Tissue Matrix AlloDerm™ RTM Perforated Rectangle sizes and thicknesses Rectangle

Product Description Piece Size (cm) Coverage (cm2) Thickness Thickness Range (mm) Product Code
AlloDerm SELECT™ Regenerative Tissue Matrix AlloDerm™ RTM Perforated Rectangle sizes and thicknesses Rectangle 16 x 20 320 Medium 1.6 ± 0.4mm 1518320
Thick 2.4 ± 0.4mm 1519320
X-Thick 3.4 ± 0.6mm 1522320
12 x 20 240 Medium 1.6 ± 0.4mm 15181220
Thick 2.4 ± 0.4mm 15191220
12 x 16 192 Medium 1.6 ± 0.4mm 15181216
Thick 2.4 ± 0.4mm 15191216
12 x 12 144 Medium 1.6 ± 0.4mm 1418144
Thick 2.4 ± 0.4mm 1419144
X-Thick 3.4 ± 0.6mm 1422144
10 x 20 200 Medium 1.6 ± 0.4mm 15181020
Thick 2.4 ± 0.4mm 15191020
10 x 16 160 Medium 1.6 ± 0.4mm 15181016
Thick 2.4 ± 0.4mm 15191016
8 x 20 160 Medium 1.6 ± 0.4mm 1518160
Thick 2.4 ± 0.4mm 1519160
X-Thick 3.4 ± 0.6mm 1522160
8 x 16 128 Thin 1.0 ± 0.2mm 1516128
Medium 1.6 ± 0.4mm 1518128
Thick 2.4 ± 0.4mm 1519128
X-Thick 3.4 ± 0.6mm 1522128
6 x 18 108 Medium 1.6 ± 0.4mm 1518108
Thick 2.4 ± 0.4mm 1519108
X-Thick 3.4 ± 0.6mm 1522108
6 x 16 96 Thin 1.0 ± 0.2mm 1516616
Medium 1.6 ± 0.4mm 1518616
Thick 2.4 ± 0.4mm 1519616
X-Thick 3.4 ± 0.6mm 1522616
8 x 12 96 Medium 1.6 ± 0.4mm 151896
Thick 1.6 ± 0.4mm 151996
X-Thick 3.4 ± 0.6mm 152296
6 x 12 72 Thin 1.0 ± 0.2mm 151672
Medium 1.6 ± 0.4mm 151872
Thick 2.4 ± 0.4mm 151972
X-Thick 3.4 ± 0.6mm 152272
4 x 16 64 Thin 1.0 ± 0.2mm 151664
Medium 1.6 ± 0.4mm 151864
Thick 2.4 ± 0.4mm 151964
X-Thick 3.4 ± 0.6mm 152264
5 x 10 50 Thin 1.0 ± 0.2mm 141650
Medium 1.6 ± 0.4mm 141850
Thick 2.4 ± 0.4mm 141950
X-Thick 3.4 ± 0.6mm 142250
4 x 12 48 X-Thin 0.55 ± 0.25mm 141448
Thin 1.0 ± 0.2mm 151648
Medium 1.6 ± 0.4mm 151848
Thick 2.4 ± 0.4mm 151948
X-Thick 3.4 ± 0.6mm 152248
4 x 7 28 X-Thin 0.55 ± 0.25mm 141428
Thin 1.0 ± 0.2mm 141628
Medium 1.6 ± 0.4mm 141828
Thick 2.4 ± 0.4mm 141928
X-Thick 3.4 ± 0.6mm 142228
2 x 12 24 X-Thick 3.4 ± 0.6mm 142224
3 x 7 21 Thin 1.0 ± 0.2mm 141621
Medium 1.6 ± 0.4mm 141821
Thick 2.4 ± 0.4mm 141921
X-Thick 3.4 ± 0.6mm 142221
2 x 4 8 X-Thin 0.55 ± 0.25mm 141408
Thin 1.0 ± 0.2mm 141608
Medium 1.6 ± 0.4mm 141808
Thick 2.4 ± 0.4mm 141908
X-Thick 3.4 ± 0.6mm 142208
1 x 4 4 X-Thin 0.55 ± 0.25mm 141404
Thin 1.0 ± 0.2mm 141604
Medium 1.6 ± 0.4mm 141804
Thick 2.4 ± 0.4mm 141904
X-Thick 3.4 ± 0.6mm 142204
1 x 2 2 X-Thin 0.55 ± 0.25mm 141402
Thin 1.0 ± 0.2mm 141602
Medium 1.6 ± 0.4mm 141802
Thick 2.4 ± 0.4mm 141902
X-Thick 3.4 ± 0.6mm 142202
1 x 1 1 X-Thick 3.4 ± 0.6mm 142201

Graftable Rectangle sizes and thickness

AlloDerm SELECT™
Regenerative Tissue Matrix Fenestrated Rectangle

Product Description Piece Size (cm) Coverage (cm2) Thickness Thickness Range (mm) Product Code
AlloDerm SELECT™ Regenerative Tissue Matrix Fenstrated Rectangle 4 x 4 16 Thin 1.0 ± 0.2mm 141616F
4 x 8 32 Thin 1.0 ± 0.2mm 141632F

AlloDerm SELECT™
Regenerative Tissue Matrix Meshed Rectangle

Product Description Piece Size (cm) Coverage (cm2) Thickness Thickness Range (mm) Product Code
AlloDerm SELECT™ Regenerative Tissue Matrix Meshed Rectangle 5 x 6 30 X-Thin 0.55 ± 0.25mm 141430M
Per Request Per Request X-Thin 0.55 ± 0.25mm 141400M

AlloDerm SELECT™
Regenerative Tissue Matrix Nonmeshed Rectangle

Product Description Piece Size (cm) Coverage (cm2) Thickness Thickness Range (mm) Product Code
AlloDerm SELECT™ Regenerative Tissue Matrix Nonmeshed Rectangle Per Request Per Request X-Thin 0.55 ± 0.25mm 141400
Per Request Per Request Thin 1.0 ± 0.2mm 141600
ALLODERM SELECTTM Regenerative Tissue Matrix Indications and  Important Safety Information 

ALLODERM SELECTTM Regenerative Tissue Matrix
INDICATIONS AND IMPORTANT SAFETY INFORMATION

INDICATIONS

ALLODERM SELECTTM Regenerative Tissue Matrix (ALLODERM SELECTTM RTM refers to both ALLODERM SELECTTM RTM and ALLODERM SELECT RESTORETM RTM products) is intended to be used for repair or replacement of damaged or inadequate integumental tissue or for other homologous uses of human integument. This product is intended for single patient one-time use only. ALLODERM SELECTTM RTM is not indicated for use as a dural substitute or intended for use in veterinary applications.

IMPORTANT SAFETY INFORMATION

CONTRAINDICATIONS

ALLODERM SELECTTM RTM should not be used in patients with a known sensitivity to any of the antibiotics listed on the package and/or Polysorbate 20.

WARNINGS

Processing of the tissue, laboratory testing, and careful donor screening minimize the risk of the donor tissue transmitting disease to the recipient patient. As with any processed donor tissue, ALLODERM SELECTTM RTM is not guaranteed to be free of all pathogens. No long-term studies have been conducted to evaluate the carcinogenic or mutagenic potential or reproductive impact of the clinical application of ALLODERM SELECTTM RTM.

DO NOT re-sterilize ALLODERM SELECTTM RTM. DO NOT reuse once the tissue graft has been removed from the packaging and/or is in contact with a patient. Discard all open and unused portions of the product in accordance with standard medical practice and institutional protocols for disposal of human tissue. Once a package or container seal has been compromised, the tissue shall be either transplanted, if appropriate, or otherwise discarded. DO NOT use if the foil pouch is opened or damaged. DO NOT use if the seal is broken or compromised. DO NOT use if the temperature monitoring device does not display “OK.” DO NOT use after the expiration date noted on the label. Transfer ALLODERM SELECTTM RTM from the foil pouch aseptically. DO NOT place the foil pouch in the sterile field.

PRECAUTIONS

Poor general medical condition or any pathology that would limit the blood supply and compromise healing should be considered when selecting patients for implanting ALLODERM SELECTTM RTM as such conditions may compromise successful clinical outcome. Whenever clinical circumstances require implantation in a site that is contaminated or infected, appropriate local and/or systemic anti-infective measures should be taken.

ALLODERM SELECTTM RTM has a distinct basement membrane (upper) and dermal surface (lower). When applied as an implant, it is recommended that the dermal side be placed against the most vascular tissue. Soak the tissue for a minimum of 2 minutes using a sterile basin and room temperature sterile saline or room temperature sterile lactated Ringer’s solution to cover the tissue. If any hair is visible, remove using aseptic technique before implantation.

ALLODERM SELECTTM RTM should be hydrated and moist when the package is opened. DO NOT use if this product is dry. Use of this product is limited to specific health professionals (e.g., physicians, dentists, and/or podiatrists). Certain considerations should be made to reduce the risk of adverse events when performing surgical procedures using a tissue graft. Please see the Instructions for Use (IFU) for more information on patient/product selection and surgical procedures involving tissue implantation before using ALLODERM SELECTTM RTM.

ADVERSE EVENTS

The most commonly reported adverse events associated with the implant of a tissue graft include, but are not limited to the following: wound or systemic infection; seroma; dehiscence; hypersensitive, allergic or other immune response; and sloughing or failure of the graft.

ALLODERM SELECTTM RTM is available by prescription only.

For more information, please see the Instructions for Use (IFU) for ALLODERM SELECTTM RTM available at www.allergan.com/AlloDermIFU or call 1.800.678.1605.

To report an adverse reaction, please call Allergan at 1.800.433.8871.

ALLODERM SELECTTM Regenerative Tissue Matrix Indications and  Important Safety Information 

ALLODERM SELECTTM Regenerative Tissue Matrix
INDICATIONS AND IMPORTANT SAFETY INFORMATION

INDICATIONS

ALLODERM SELECTTM Regenerative Tissue Matrix (ALLODERM SELECTTM RTM refers to both ALLODERM SELECTTM RTM and ALLODERM SELECT RESTORETM RTM products) is intended to be used for repair or replacement of damaged or inadequate integumental tissue or for other homologous uses of human integument. This product is intended for single patient one-time use only. ALLODERM SELECTTM RTM is not indicated for use as a dural substitute or intended for use in veterinary applications.

IMPORTANT SAFETY INFORMATION

CONTRAINDICATIONS

ALLODERM SELECTTM RTM should not be used in patients with a known sensitivity to any of the antibiotics listed on the package and/or Polysorbate 20.

WARNINGS

Processing of the tissue, laboratory testing, and careful donor screening minimize the risk of the donor tissue transmitting disease to the recipient patient. As with any processed donor tissue, ALLODERM SELECTTM RTM is not guaranteed to be free of all pathogens. No long-term studies have been conducted to evaluate the carcinogenic or mutagenic potential or reproductive impact of the clinical application of ALLODERM SELECTTM RTM.

DO NOT re-sterilize ALLODERM SELECTTM RTM. DO NOT reuse once the tissue graft has been removed from the packaging and/or is in contact with a patient. Discard all open and unused portions of the product in accordance with standard medical practice and institutional protocols for disposal of human tissue. Once a package or container seal has been compromised, the tissue shall be either transplanted, if appropriate, or otherwise discarded. DO NOT use if the foil pouch is opened or damaged. DO NOT use if the seal is broken or compromised. DO NOT use if the temperature monitoring device does not display “OK.” DO NOT use after the expiration date noted on the label. Transfer ALLODERM SELECTTM RTM from the foil pouch aseptically. DO NOT place the foil pouch in the sterile field.

PRECAUTIONS

Poor general medical condition or any pathology that would limit the blood supply and compromise healing should be considered when selecting patients for implanting ALLODERM SELECTTM RTM as such conditions may compromise successful clinical outcome. Whenever clinical circumstances require implantation in a site that is contaminated or infected, appropriate local and/or systemic anti-infective measures should be taken.

ALLODERM SELECTTM RTM has a distinct basement membrane (upper) and dermal surface (lower). When applied as an implant, it is recommended that the dermal side be placed against the most vascular tissue. Soak the tissue for a minimum of 2 minutes using a sterile basin and room temperature sterile saline or room temperature sterile lactated Ringer’s solution to cover the tissue. If any hair is visible, remove using aseptic technique before implantation.

ALLODERM SELECTTM RTM should be hydrated and moist when the package is opened. DO NOT use if this product is dry. Use of this product is limited to specific health professionals (e.g., physicians, dentists, and/or podiatrists). Certain considerations should be made to reduce the risk of adverse events when performing surgical procedures using a tissue graft. Please see the Instructions for Use (IFU) for more information on patient/product selection and surgical procedures involving tissue implantation before using ALLODERM SELECTTM RTM.

ADVERSE EVENTS

The most commonly reported adverse events associated with the implant of a tissue graft include, but are not limited to the following: wound or systemic infection; seroma; dehiscence; hypersensitive, allergic or other immune response; and sloughing or failure of the graft.

ALLODERM SELECTTM RTM is available by prescription only.

For more information, please see the Instructions for Use (IFU) for ALLODERM SELECTTM RTM available at www.allergan.com/AlloDermIFU or call 1.800.678.1605.

To report an adverse reaction, please call Allergan at 1.800.433.8871.