510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K011796Substantially Equivalent

Renu Multiplus No Rub Multi-Purpose Solution

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

K011796 is the FDA 510(k) clearance record for RENU MULTIPLUS NO RUB MULTI-PURPOSE SOLUTION, a class II device, cleared for Bausch & Lomb, Inc. on under FDA product code LPN (Accessories, Soft Lens Products). FDA records list 131 510(k) clearances for Bausch & Lomb Incorporated, from to . As of , FDA records show no recalls naming K011796.

Clearance record

Decision date
Received
(146 days to decision)
Product code
LPN Accessories, Soft Lens Products
Regulation
21 CFR 886.5928
Device class
Class II
Review panel
Ophthalmic
Applicant
Bausch & Lomb, Inc. 1400 N. Goodman St., Rochester NY
510(k) summary
Summary
Third party review
No

Clearances, product code LPN

Trailing 12 months
1 clearance under product code LPN in the twelve months to November 2026, August 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code LPN, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20261
September 20260
October 20260
November 20260