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Keratoprosthesis, Temporary Implant, Surgical Use

FDA product code MLP · 5 cleared devices

Class 2 Ophthalmic
Regulation
21 CFR 886.3400
Review panel
OP
Implant
Yes
Life sustaining
No
Third party review
Yes
GMP exempt
No
Clearance span
1984-12-18 – 2026-07-24
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