Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Device, Analysis, Anterior Segment

FDA product code MXK · 22 cleared devices

Class 2 Ophthalmic
Regulation
21 CFR 886.1850
Review panel
OP
Implant
No
Life sustaining
No
Third party review
Yes
GMP exempt
No
Clearance span
1999-03-05 – 2026-03-13
↑