FDA Device Intelligence
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Illuminator, Fiberoptic, Surgical Field

FDA product code HBI · Class 2 · General, Plastic Surgery

114
Registered devices
58
Adverse events
0
Recalls
28
510(k) clearances

Devices with this code

Fiber Optic Light Cable — GULF FIBEROPTICS, INC.Strauss Surgical — AMERICAN MEDICAL ENDOSCOPY, INC.Fiber Optic Light Cable — GULF FIBEROPTICS, INC.Fiber Optic Light Cable — GULF FIBEROPTICS, INC.Vital Vue — Covidien LPFiber Optic Light Cable — GULF FIBEROPTICS, INC.Olympus — OLYMPUS Winter & Ibe GmbHFiber Optic Light Cable — GULF FIBEROPTICS, INC.Fiber Optic Light Cable — GULF FIBEROPTICS, INC.Fiber Optic Light Cable — GULF FIBEROPTICS, INC.OptiLux LED Illuminator — Medical Illumination International Inc.Strauss Surgical — AMERICAN MEDICAL ENDOSCOPY, INC.Fiber Optic Light Cable — GULF FIBEROPTICS, INC.Fiber Optic Light Cable — GULF FIBEROPTICS, INC.Fiber Optic Light Cable — GULF FIBEROPTICS, INC.Strauss Surgical — AMERICAN MEDICAL ENDOSCOPY, INC.Fiber Optic Light Cable — GULF FIBEROPTICS, INC.Fiber Optic Light Cable — GULF FIBEROPTICS, INC.Fiber Optic Light Cable — GULF FIBEROPTICS, INC.Fiber Optic Light Cable — GULF FIBEROPTICS, INC.Strauss Surgical — AMERICAN MEDICAL ENDOSCOPY, INC.Fiber Optic Light Cable — GULF FIBEROPTICS, INC.Fiber Optic Light Cable — GULF FIBEROPTICS, INC.Fiber Optic Light Cable — GULF FIBEROPTICS, INC.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.