DEVICE CLASS
Class II
REGULATION
21 CFR 886.5916
MEDICAL SPECIALTY
Ophthalmic
REVIEW PANEL
OP
— Implant— Life-sustaining— GMP-exempt✓ Third-party review eligible
3
510(K)/PMA CLEARANCES
510k: 3
0
RECALL ENTRIES
Recent clearances
K253822Zhuhai Fitlens Medical Technology Co., Ltd. · 510k2026-03-27
K242393Acuity Polymers, Inc. · 510k2024-11-01
K241398Tianjin Mastervision Technology Co., Ltd. · 510k2024-10-22
Related on SPEQ
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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