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LEONE SPA

LEONE SPA · Model P1600-95 · UDI-DI 08033707069287

ECQ Prescription
2
510(k) clearances
5
Adverse events
1
Recalls
85
Facilities

Description

BRACKET POSITIONING GAUGE KIT

Recalls

DateFirmReason
2013-11-13Karl Storz Endoscopy America IncKARL STORZ Endoscopy America, Inc. is recalling the Flexible Broncho Fiberscope or a Flexible Intubation Fiberscope with a suction port because the material used in the suction cha

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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.