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Helios Biomedical, Inc.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories2
Latest Approval2025-08-15
TypeNumberDevice NameCodeDate
510(k) K250397 Helios Dermal Scaffold KGN 2025-08-15 View
510(k) K250420 Helios Dura Regeneration Matrix GXQ 2025-05-14 View
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