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Endoform™ Natural Restorative Bioscaffold

AROA BIOSURGERY LIMITED · Model 529311 · UDI-DI 09421906017281

KGN Prescription
1
510(k) clearances
185
Adverse events (1 deaths)
23
Recalls
136
Facilities

Description

Endoform™ Natural is a 100% w/w intact extracellular matrix (ECM), manufactured from ovine (sheep) forestomach tissue. This advanced wound care device retains the innate biological structure of the native ECM, along with associated macromolecules including elastin, fibronectin, glycosaminoglycans and laminin. When rehydrated with wound exudate or sterile saline, Endoform Natural transforms into a soft conforming sheet, which is incorporated into the wound over time.

Recalls

DateFirmReason
2026-03-19Integra LifeSciences Corp. (NeuroSciences)Increased rate of out-of-specification endotoxin results.
2026-03-19Integra LifeSciences Corp. (NeuroSciences)Increased rate of out-of-specification endotoxin results.
2026-03-19Integra LifeSciences Corp. (NeuroSciences)Increased rate of out-of-specification endotoxin results.
2026-03-19Integra LifeSciences Corp. (NeuroSciences)Increased rate of out-of-specification endotoxin results.
2026-03-19Integra LifeSciences Corp. (NeuroSciences)Increased rate of out-of-specification endotoxin results.
2026-02-10Medline Industries, LPElevated endotoxin levels identified in affected lots. Issue may elicit strong inflammatory response if used, including local tissue irritation, delayed wound healing, or systemic
2023-05-23TEI Biosciences, Inc.Possible out of specification endotoxin test results due to issues with in-process and finished goods endotoxin testing.
2023-05-23TEI Biosciences, Inc.Possible out of specification endotoxin test results due to issues with in-process and finished goods endotoxin testing.
2023-05-23TEI Biosciences, Inc.Possible out of specification endotoxin test results due to issues with in-process and finished goods endotoxin testing.
2023-05-23TEI Biosciences, Inc.Possible out of specification endotoxin test results due to issues with in-process and finished goods endotoxin testing.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.