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Spotter Device Set

FORUM ENGINEERING TECHNOLOGIES (96) LTD. · Model SPR · UDI-DI 17290114352007

LNF Prescription
0
510(k) clearances
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Adverse events
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Recalls
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Facilities

Description

Spotter Device set

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.