Amo Puerto Rico Manufacturing, Inc
Road 402 N., Industrial Park, ANASCO, PR, US
Registered product codes
6 product codes
Recent MDR events
1 on file
Recalls
19 on file
- Open, ClassifiedMar 24, 2026
Due to identifying a limited quantity of intraocular lenses that may have a haptic that sticks to the optic which prevents the lens from unfolding as consistently as expected.
View FDA record ↗ - TerminatedAug 26, 2014
Units may be labeled with the incorrect diopter power.
View FDA record ↗ - TerminatedAug 26, 2014
Units may be labeled with the incorrect diopter power.
View FDA record ↗ - TerminatedAug 26, 2014
Units may be labeled with the incorrect diopter power.
View FDA record ↗ - TerminatedAug 26, 2014
Units may be labeled with the incorrect diopter power.
View FDA record ↗ - TerminatedAug 26, 2014
Units may be labeled with the incorrect diopter power.
View FDA record ↗ - TerminatedAug 26, 2014
Units may be labeled with the incorrect diopter power.
View FDA record ↗ - TerminatedAug 26, 2014
Units may be labeled with the incorrect diopter power.
View FDA record ↗ - TerminatedAug 26, 2014
Units may be labeled with the incorrect diopter power.
View FDA record ↗ - TerminatedAug 26, 2014
Units may be labeled with the incorrect diopter power.
View FDA record ↗
Compliance history
Matched by FEI 2648035.
FDA inspections
0 on file
No inspections on file for this FEI number.
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.