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Earlens Hybrid Impression Kit

EARLENS CORPORATION · Model HIK02 · UDI-DI 00850013007349

LDG Prescription
2
510(k) clearances
13
Adverse events
0
Recalls
8
Facilities

Description

Includes - Medial Impression Cartridges - Lateral Impression Cartridges - Medial Mixing Tips - Lateral Mixing Tips

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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.