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FENTEX

FENTEX medical GmbH · Model 711173FX · UDI-DI 04250407748890

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510(k) clearances

Adverse events

Recalls

Facilities

Description

Storz Adapter for Standard telescopes

Recalls

Date	Firm	Reason
2007-02-07	Boston Scientific Corporation	Light Degradation in transmission-A film may deposit on the front face and limit transmission of light

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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.