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Karl Storz GmbH & Co. KG · Model 20161220 · UDI-DI 04048551317488

NTN Prescription

510(k) clearances

273

Adverse events

Recalls

Facilities

Description

LED Nova 150, without accessories

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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.