Newly Approved


Dual Layer Membrane
Awarded Q Code Q4262 (effective 1/1/23)

Dual Layer Impax Membrane is a sterile allograft designed for optimal wound covering and protection during the treatment of wounds.
Dual Layer Impax Membrane Key Features and Properties
  • Provides a protective wound covering
  • Dehydrated extracellular matrix acts as a scaffold supporting the native tissue
  • Adheres easily to wounds, including those with irregular surfaces
  • Immune privileged and angiogenic
  • 5-year shelf life at ambient temperature storage

Impax Ordering Information

IMP-0202 2×2 4
IMP-0203 2×3 6
IMP-0404 4×4 16
IMP-0406 4×6 24
IMP-0408 4×8 32
IMP-1020 10×20 200
IMP-1520 15×20 300

Dual Layer Impax Membrane is an amniotic membrane allograft derived from a prescreened mother with a planned C-section delivery. Dual Layer Impax Membrane is manufactured in compliance with FDA regulations and AATB guidance. The membrane is minimally processed to preserve the native structure of the tissue, dehydrated, and terminally sterilized. Dual Layer Impax Membrane is confirmed by the FDA Tissue Reference Group to meet the criteria for regulation solely under Section 361 of the PHS Act as defined in 21 CFR Part 1271.

Legacy Medical Consultants is an integrated marketer of proprietary regenerative biomaterial products processed from human amniotic membrane and other birth tissues. Only qualified health professionals should implant biomaterial products including amniotic grafts. This website is not meant as a substitute for professional medical advice.
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