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AlloDermTM Regenerative Tissue Matrix
portfolio of products

AlloDermTM RTM is an acellular dermal matrix (ADM) that has been trusted with more than 3 million implantations.1 No other ADM has more publications, with hundreds of scientific* and clinical articles.2 And no other ADM has the extensive experience of AlloDermTM RTM—25 years and counting.3 AlloDermTM RTM offers a wide range of products to meet your needs

Sterile4

Zero documented disease transmissions5

Ready to use with a minimum 2-minute soak4

Able to be stored without refrigeration4

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

Implantable

Perforated

AlloDerm™ 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

Perforated Contour: Sizes and thicknesses

AlloDerm SELECT™
Regenerative Tissue Matrix    Perforated Contour

Product description Piece size (cm) Coverage (cm2) Thickness Thickness range (mm) Product code
AlloDerm SELECT™ Regenerative Tissue Matrix   Perforated Contour X-Large
11.8 x 23.7
200 Medium 1.6 ± 0.4 CXL1519P
Thick 2.4 ± 0.4 CXL1518P
Large
10.7 x 21.5
164 Thin 1.0 ± 0.2 CL1516P
Medium 1.6 ± 0.4 CL1518P
Thick 2.4 ± 0.4 CL1519P
Medium
9.6 x 19.3
132 Thin 1.0 ± 0.2 CM1516P
Medium 1.6 ± 0.4 CM1518P
Thick 2.4 ± 0.4 CM1519P
Small
7.3 x 14.7
77 Thin 1.0 ± 0.2 CS1516P
Medium 1.6 ± 0.4 CS1518P
Thick 2.4 ± 0.4 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 ± 0.4 CXL1518
Thick 2.4 ± 0.4 CXL1519
Large
10.7 x 21.5
164 Thin 1.0 ± 0.2 CL1516
Medium 1.6 ± 0.4 CL1518
Thick 2.4 ± 0.4 CL1519
Medium
9.6 x 19.3
132 Thin 1.0 ± 0.2 CM1516
Medium 1.6 ± 0.4 CM1518
Thick 2.4 ± 0.4 CM1519
Small
7.3 x 14.7
77 Thin 1.0 ± 0.2 CS1516
Medium 1.6 ± 0.4 CS1518
Thick 2.4 ± 0.4 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 ± 0.4 1518320P
Thick 2.4 ± 0.4 1519320P
X-Thick 3.4 ± 0.6 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 ± 0.4 1518320
Thick 2.4 ± 0.4 1519320
X-Thick 3.4 ± 0.6 1522320
12 x 20 240 Medium 1.6 ± 0.4 15181220
Thick 2.4 ± 0.4 15191220
12 x 16 192 Medium 1.6 ± 0.4 15181216
Thick 2.4 ± 0.4 15191216
12 x 12 144 Medium 1.6 ± 0.4 1418144
Thick 2.4 ± 0.4 1419144
X-Thick 3.4 ± 0.6 1422144
10 x 20 200 Medium 1.6 ± 0.4 15181020
Thick 2.4 ± 0.4 15191020
10 x 16 160 Medium 1.6 ± 0.4 15181016
Thick 2.4 ± 0.4 15191016
8 x 20 160 Medium 1.6 ± 0.4 1518160
Thick 2.4 ± 0.4 1519160
X-Thick 3.4 ± 0.6 1522160
8 x 16 128 Thin 1.0 ± 0.2 1516128
Medium 1.6 ± 0.4 1518128
Thick 2.4 ± 0.4 1519128
X-Thick 3.4 ± 0.6 1522128
6 x 18 108 Medium 1.6 ± 0.4 1518108
Thick 2.4 ± 0.4 1519108
X-Thick 3.4 ± 0.6 1522108
6 x 16 96 Thin 1.0 ± 0.2 1516616
Medium 1.6 ± 0.4 1518616
Thick 2.4 ± 0.4 1519616
X-Thick 3.4 ± 0.6 1522616
8 x 12 96 Medium 1.6 ± 0.4 151896
Thick 1.6 ± 0.4 151996
X-Thick 3.4 ± 0.6 152296
6 x 12 72 Thin 1.0 ± 0.2 151672
Medium 1.6 ± 0.4 151872
Thick 2.4 ± 0.4 151972
X-Thick 3.4 ± 0.6 152272
4 x 16 64 Thin 1.0 ± 0.2 151664
Medium 1.6 ± 0.4 151864
Thick 2.4 ± 0.4 151964
X-Thick 3.4 ± 0.6 152264
5 x 10 50 Thin 1.0 ± 0.2 141650
Medium 1.6 ± 0.4 141850
Thick 2.4 ± 0.4 141950
X-Thick 3.4 ± 0.6 142250
4 x 12 48 X-Thin 0.55 ± 0.25 141448
Thin 1.0 ± 0.2 151648
Medium 1.6 ± 0.4 151848
Thick 2.4 ± 0.4 151948
X-Thick 3.4 ± 0.6 152248
4 x 7 28 X-Thin 0.55 ± 0.25 141428
Thin 1.0 ± 0.2 141628
Medium 1.6 ± 0.4 141828
Thick 2.4 ± 0.4 141928
X-Thick 3.4 ± 0.6 142228
2 x 12 24 X-Thick 3.4 ± 0.6 142224
3 x 7 21 Thin 1.0 ± 0.2 141621
Medium 1.6 ± 0.4 141821
Thick 2.4 ± 0.4 141921
X-Thick 3.4 ± 0.6 142221
2 x 4 8 X-Thin 0.55 ± 0.25 141408
Thin 1.0 ± 0.2 141608
Medium 1.6 ± 0.4 141808
Thick 2.4 ± 0.4 141908
X-Thick 3.4 ± 0.6 142208
1 x 4 4 X-Thin 0.55 ± 0.25 141404
Thin 1.0 ± 0.2 141604
Medium 1.6 ± 0.4 141804
Thick 2.4 ± 0.4 141904
X-Thick 3.4 ± 0.6 142204
1 x 2 2 X-Thin 0.55 ± 0.25 141402
Thin 1.0 ± 0.2 141602
Medium 1.6 ± 0.4 141802
Thick 2.4 ± 0.4 141902
X-Thick 3.4 ± 0.6 142202
1 x 1 1 X-Thick 3.4 ± 0.6 142201

Graftable Rectangle: Sizes and thicknesses

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 Fenestrated Rectangle 4 x 4 16 Thin 1.0 ± 0.2 141616F
4 x 8 32 Thin 1.0 ± 0.2 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 ± 0.25 141430M
Per request Per request X-Thin 0.55 ± 0.25 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 ± 0.25 141400
Per request Per request Thin 1.0 ± 0.2 141600
References: 1. Data on file, Allergan Aesthetics, 2021; Number of AlloDermTM RTM Units Sold. 2. Data on file, Allergan Aesthetics; Search Performed on PubMed in August 2021. 3. Wainwright DJ. Use of an acellular allograft dermal matrix (AlloDerm) in the management of full-thickness burns. Burns. 1995;21(4):243-248. 4. AlloDerm SELECTTM and AlloDerm SELECT RESTORETM Regenerative Tissue Matrix Instructions for Use, March 2020. 5. Data on file, Allergan Aesthetics, October 2021. 6. Data on file, Allergan; Study Report LRD2015-05-002. 7. Data on file, Allergan; Study Report LRD2012-10-005.
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 SELECTDTM 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.

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