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Organogenesis Holdings Inc

Organogenesis Holdings Inc., a regenerative medicine company, develops, manufactures, and commercializes products for the advanced wound care, and surgical and sports medicine markets in the United States. Its advanced wound care products include Affinity and Novachor, which are amnion and chorion placental allografts for use in the care of chronic and acute wounds as protective barriers and extracellular matrix (ECM) scaffolds; Apligraf, a bioengineered bi-layered skin substitute for the treatment of venous leg ulcers and diabetic foot ulcers (DFU); Dermagraft, a dermal substitute grown from human dermal fibroblasts to treat DFUs; NuShield, a dehydrated placental allograft and surgical barrier to provide a protective barrier and ECM scaffold to support native healing; PuraPly Antimicrobial (AM) and PuraPly SX, which are antimicrobial barriers for the management of open wounds in surgical settings; and CYGNUS Dual, VIA Matrix, and SimpliMax are placental tissue grafts used to treat chronic and acute wounds that can be stored at room temperature. The company also provides PuraPly MZ, a micronized version of PuraPly for the management of open wounds in surgical settings; PuraForce, a bioengineered porcine collagen surgical matrix for use in soft tissue reinforcement applications; FortiShield, a biosynthetic wound matrix for use as a temporary protective covering; and TransCyte, a bioengineered tissue scaffold that promotes burn healing. In addition, it develops ReNu, a cryopreserved suspension, which is in Phase 3 trial, for the management of symptoms associated with knee osteoarthritis; and placental products. The company serves hospitals, wound care centers, government facilities, ambulatory service centers, and physician offices through direct sales representatives and independent agencies. Organogenesis Holdings Inc. is headquartered in Canton, Massachusetts.

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Organogenesis Holdings reports second quarter 2026 net loss of $96.3 million

Organogenesis Holdings reported a net loss of $96.3 million for the second quarter of 2026, compared to a net loss of $9.4 million in the same period last year. Net revenue fell 58% to $42.8 million, driven by a 61% decline in Advanced Wound Care product revenue to $36.1 million, while Surgical & Sports Medicine revenue decreased 18% to $6.7 million. The company also lowered its full-year 2026 revenue guidance to between $179 million and $215 million, representing a decline of 62% to 68% from 2025. Adjusted EBITDA loss widened to $34.4 million from $3.6 million a year earlier. Cash and equivalents stood at $46.8 million with no outstanding debt as of June 30, 2026.
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Biotech & Genomic Medicine

Organogenesis' ReNu knee OA therapy accepted for FDA review

Organogenesis Holdings announced that the U.S. FDA has accepted its Biologics License Application for ReNu, a cryopreserved amniotic suspension allograft for managing pain in symptomatic knee osteoarthritis. The FDA set a PDUFA action date of April 24, 2027. ReNu combines amniotic fluid cells and micronized amniotic membrane and has been studied in three large randomized controlled trials involving over 1,300 patients. The therapy previously received FDA RMAT designation in 2021. The FDA also conditionally accepted Amnuvx as the proprietary name for ReNu, pending final review and approval.
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Biotech & Genomic Medicine

Regenerative Medicine Market Projected to Surpass $100 Billion Within a Decade

The regenerative medicine market is projected to surpass US$100 billion within roughly a decade, driven by a shift from tissue replacement to regeneration using biomaterials, cell therapies, and 3D bioprinting. Independent estimates place the broad market in the tens of billions of dollars in 2026, with compound annual growth rates frequently estimated in the high teens to mid-20s percent. Key drivers include aging populations, the diabetes epidemic, rising surgical volumes, and growing demand in aesthetics, partly fueled by GLP-1 weight-loss medications. The sector spans profitable commercial leaders like Integra LifeSciences and Vericel to early-stage platform companies such as Conexeu Sciences, which began trading on Nasdaq in May 2026 with its collagen-based extracellular-matrix platform. Reimbursement policy and regulatory pathways remain critical risks, as illustrated by recent upheaval in the U.S. skin-substitute market affecting companies like Organogenesis and MiMedx.
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