International safety notice

General name: Multifocal posterior chamber lens Sales name: Lentis Comfort

Japan / PMDA Recalls · JPN · Jul 18, 2025

Key facts

Regulator Japan / PMDA Recalls
Country JPN
Brand General name: Multifocal posterior chamber lens Sales name: Lentis Comfort
Manufacturer Santen Pharmaceutical Co., Ltd.
Models 50914354012, 50914354026, 50914354017, 50913245002, 50914354023, 50914354008, 50914354003, LS-313, 50914354013, 50913248013, 50914354019, 50914354025 and 44 more
Date Jul 18, 2025
Regulator page info.pmda.go.jp

At a glance

  • No Recall
  • No Field safety notice

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About International device safety notices

Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.

Source: National medical device regulators (as listed), compiled by Orca1

Browse all International device safety notices