510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K132715Substantially Equivalent

Bausch + Lomb Bioture Oneday for Presbyopia (Nesofilcon a) Contact Lens

Bausch & Lomb Incorporated, Rochester NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K132715 is the FDA 510(k) clearance record for BAUSCH + LOMB BIOTURE ONEDAY FOR PRESBYOPIA (NESOFILCON A) CONTACT LENS, a class II device, cleared for Bausch & Lomb, Incorporated on under FDA product code LPL (Lenses, Soft Contact, Daily Wear). FDA records list 131 510(k) clearances for Bausch & Lomb, Incorporated, from to . As of , FDA records show no recalls naming K132715.

Clearance record

Decision date
Received
(112 days to decision)
Product code
LPL Lenses, Soft Contact, Daily Wear
Regulation
21 CFR 886.5925
Device class
Class II
Review panel
Ophthalmic
Applicant
Bausch & Lomb, Incorporated 1400 N. Goodman St., Rochester NY
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LPL

Trailing 12 months
9 clearances under product code LPL in the twelve months to October 2026, May 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code LPL, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20261
March 20262
April 20261
May 20263
June 20260
July 20260
August 20260
September 20261
October 20260