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FDA PRODUCT CODE · CLASS III

POE — Extended Depth Of Focus Intraocular Lens

Intended to be implanted to replace the natural lens of an eye.

DEVICE CLASS
Class III
REGULATION
21 CFR 886.3600
MEDICAL SPECIALTY
Ophthalmic
REVIEW PANEL
OP
✓ Implant— Life-sustaining— GMP-exempt— Third-party review eligible
1
510(K)/PMA CLEARANCES
pma: 1
0
RECALL ENTRIES

Recent clearances

P210005Acu Focus, Inc. · pma2026-07-14

Related on SPEQ

Medical devices industry →Medical device quality (ISO 13485) →FDA device clearances →FDA enforcement & recalls →

Source: FDA device classification, 510(k)/PMA, and recall datasets (openFDA). Recall entries count distinct FDA recall numbers, so one recall event affecting several products appears as several entries. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data.

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