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Device, Communications, Images, Ophthalmic
FDA product code NFG · Class 1 · Radiology
13
Registered devices
39
Adverse events
1
Recalls
0
510(k) clearances
Devices with this code
VERION™ — Alcon Laboratories, Inc.Image filing software NAVIS-EX — NIDEK CO.,LTD.INTEGRATION BROKER — Smith & Nephew, Inc.Cassini Guidance System — Cassini Technologies B.V.Image filing software — NIDEK CO.,LTD.N/A — Smith & Nephew, Inc.Optina Fotys — Optina Diagnostiques, IncINTEGRATION BROKER — Smith & Nephew, Inc.NON-MYDRIATIC AUTO FUNDUS CAMERA — NIDEK CO.,LTD.CANON INC. — CANON INC.Navilas® Laser System 577s — OD-OS GmbHFORUM Viewer App — Carl Zeiss Meditec AGVISUPAC 500 — Carl Zeiss Meditec AG
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2016-03-01 | Alcon Research, Ltd. | Alcon is conducting a voluntary medical device correction of all VERION Reference Units (Vision Planner) that are shared with the Alcon LenSx Laser System after |
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