Bausch + Lomb, Incorporated

FDA Regulatory Profile

Bausch + Lomb, Incorporated appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on November 17, 2023.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Known Names

bausch & lomb incorporated, bausch & lomb, incorporated, bausch + lomb, incorporated

Recent 510(k) Clearances

K-NumberDeviceDate
K230954Samfilcon B Custom Contact LensNovember 17, 2023
K211786Independent Corneal Viewing Chamber (IVC-21)December 3, 2021
K200528Bausch + Lomb (Kalifilcon A) Soft Contact Lens, Bausch + Lomb (Kalifilcon A) Soft Contact Lens for aJune 2, 2020
K171404BOSTON XO (hexafocon A), BOSTON XO2 (hexafocon B)July 17, 2017