FDA Device Intelligence
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Probe, Lachrymal

FDA product code HNL · Class 1 · Ophthalmic

654
Registered devices
40
Adverse events
1
Recalls
10
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2015-02-26Quest Medical, Inc.Expiration date incorrectly printed in Manufacturing Date field on both pouch and carton labels

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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