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OsteoPoint

Morpheus AG · Model HCT-04-160 · UDI-DI 04260647240344

HAE
10
510(k) clearances
482
Adverse events (1 deaths)
2
Recalls
64
Facilities

Description

HC Biologics OsteoPoint Bone Removal System 4mm x 160mm

Recalls

DateFirmReason
2023-10-30Folsom Metal Products, Inc.Units were not intended for commercial distribution and inadvertently distributed.
2023-10-30Folsom Metal Products, Inc.Units were not intended for commercial distribution and inadvertently distributed.

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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.