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Arrowhead DE LLC

1 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
Arrow-LOK Implant, REF: 21-253519, 21-253522, 21-253525, 21-253528, 21-253530, 21-253533, recall (Z-2958-2026)Arrowhead DE LLC2026-08-14

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