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RONIN

Ronin Surgical Corp. · Model X6 · UDI-DI 00850061395009

HPP Prescription
0
510(k) clearances
12
Adverse events
1
Recalls
71
Facilities

Description

HEADLAMP, OPERATING, BATTERY-OPERATED

Recalls

DateFirmReason
2014-06-11Integra LifeSciences Corp.LED battery chargers may prematurely fail and will not charge the LED battery as intended

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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.