510(k) Report

PMA · Approved

Approved

Bausch & Lomb Renew (R) Saline Soln. (BL-101-BEU13

P800024/S016PMAApproved Feb 28, 1991331-day reviewClass II21 CFR 886.5928

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Bausch & Lomb, Inc. · LPN Accessories, Soft Lens Products

Approved on Feb 28, 1991 through premarket approval, which rests on the device’s own clinical evidence after a 331-day review. 3 later devices descend from it.

Decided
Feb 28, 1991
Review
331 days
Class
Class II
Product code
LPN
Recalls
None

3 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2017: 2 descendants cleared2018: 1 descendant cleared1990200020102020
  1. This deviceP800024/S016 Bausch & Lomb Renew (R) Saline Soln. (BL-101-BEU13Bausch & Lomb, Inc. · 1991
  2. Descendant · cites it directly · 2 of its ownK170483 Bausch + Lomb Sensitive Eyes Plus Saline SolutionBausch & Lomb, Incorporated · 2017
  3. Descendant · 2 generations on · 0 of its ownK180319 Bausch + Lomb Boston Advance Cleaner, Bausch + Lomb Boston Advance…Bausch and Lomb, Incorporated · 2018
  4. Descendant · 2 generations on · 0 of its ownK173089 Bausch + Lomb Boston Original Cleaner, Bausch + Lomb Boston Original…Bausch & Lomb, Incorporated · 2017

Most influential descendants

Showing 3 of 3 · See all
  • K170483Bausch + Lomb Sensitive Eyes Plus Saline SolutionBausch & Lomb, Incorporated · 2017 · cites it directly2descendants
  • K180319Bausch + Lomb Boston Advance Cleaner, Bausch + Lomb Boston Advance Conditioning SolutionBausch and Lomb, Incorporated · 2018 · 2 generations on0descendants
  • K173089Bausch + Lomb Boston Original Cleaner, Bausch + Lomb Boston Original Conditioning…Bausch & Lomb, Incorporated · 2017 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)P800024/S016Bausch & Lomb Renew (R) Saline Soln. (BL-101-BEU13Bausch & Lomb, Inc.1991—
+1K170483Bausch + Lomb Sensitive Eyes Plus Saline SolutionBausch & Lomb, Incorporated2017—
+2K180319Bausch + Lomb Boston Advance Cleaner, Bausch + Lomb Boston Advance…Bausch and Lomb, Incorporated2018—
+2K173089Bausch + Lomb Boston Original Cleaner, Bausch + Lomb Boston Original…Bausch & Lomb, Incorporated2017—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201720
201810
FIG. 1 — Lineage of P800024/S016, 1991–2018Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA PMA database (decision fields and supplements), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in LPN? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new LPN device

  1. #1 K253795 MeniSept 3% Hydrogen Peroxide Cleaning &…score 12.7 · 4 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

Does it have a predicate?

PMA decisions do not claim a predicate device.

What descends from it? (3)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K170483Bausch + Lomb Sensitive Eyes Plus Saline SolutionBausch & Lomb, Incorporated20172

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • Of its descendants, K170483 (Bausch & Lomb, Incorporated, 2017) has gone furthest, with 2 descendants of its own.

How does its category compare?

All LPN devices

LPN Accessories, Soft Lens Products: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · LPN

2in 2022

2007: 42009: 12010: 22011: 32012: 22013: 22015: 22016: 32017: 12019: 22020: 32021: 22022: 22026 (partial year): 1
2007high 4 (2007) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LPN

167in 2020

2007: 175 days median2011: 222 days median2016: 59 days median2020: 167 days median
2007high 222 (2011) · low 59 (2016)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · LPN

1in 2020

2007: 22009: 22010: 22011: 12016: 12020: 1
2007high 2 (2007) · low 0 (2008)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · LPN

40in 2025

2007: 1,1512008: 1532009: 1212010: 2412011: 2732012: 2682013: 842014: 1052015: 1762016: 4982017: 2,6662018: 952019: 602020: 822021: 512022: 622023: 842024: 762025: 40
2007high 2,666 (2017) · low 40 (2025)2025

MAUDE reports naming product code LPN, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
2007417521,151
20080—0153
20091—2121
20102—2241
201132221273
20122—0268
20132—084
20140—0105
20152—0176
20163591498
20171—02,666
20180—095
20192—060
20203167182
20212—051
20222—062
20230—084
20240—076
20250—040
20261—0—
Cite this page

510(k) Report. “P800024/S016: Bausch & Lomb Renew (R) Saline Soln. (BL-101-BEU13.” Lineage record from FDA PMA data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/P800024/S016

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026