MLPClass IIImplant

Keratoprosthesis, Temporary Implant, Surgical Use

Ophthalmic · 21 CFR 886.3400

MDR events2All time

Recalls0All time

Registered firms3Currently listed

510(k) clearances5All time

Recent MDR events

2 adverse event reports on file

Event type breakdown

Injury1

Other1

Most-reported manufacturers

Unspecified1 Coopervision Surgical1

Recalls

0 recall events for this product code

No recalls on file for this product code.

Registered firms

3 firms currently registered for this product code

510(k) clearances

5 clearances for this product code