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U.S. Department of Health and Human Services

Establishment Registration & Device Listing

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Proprietary Name: BioFoam Surgical Matrix
Classification Name: AGENT, ABSORBABLE HEMOSTATIC, NON-COLLAGEN BASED
Product Code: LMG
Device Class: 3
Regulation Number: 878.4490
Medical Specialty: General & Plastic Surgery
Registered Establishment Name: CryoLife
Registered Establishment Number: 1063481
Owner/Operator: CryoLife
Owner/Operator Number: 9003683
Establishment Operations: U.S. Manufacturer of Export Only Devices
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