510(k) · Cleared
ClearedComplete Brand Multi-Purpose Solution
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Advanced Medical Optics, Inc. · LPN Accessories, Soft Lens Products
Cleared on Apr 4, 2003 after an 84-day review. The FDA summary names no predicate by number. 3 later devices descend from it.
- Decided
- Apr 4, 2003
- Review
- 84 days
- Class
- Class II
- Product code
- LPN
- Recalls
- None
- Predicates
- 0
3 later devices descend from it, 2 citing it directly.
- This deviceK030092 Complete Brand Multi-Purpose SolutionAdvanced Medical Optics, Inc. · 2003
- Descendant · cites it directly · 1 of its ownK051104 Eye See Multipurpose, NO-Rub Contact Lens SolutionLapis Lazuli, NV · 2006
- Descendant · cites it directly · 0 of its ownK161819 NNR06 Multi-Purpose SolutionBausch & Lomb, Incorporated · 2016
- Descendant · 2 generations on · 0 of its ownK070767 Eye See Multipurpose Contact Lens SolutionLapis Lazuli International NV · 2007
Most influential descendants
Showing 3 of 3 · See all- K051104Eye See Multipurpose, NO-Rub Contact Lens SolutionLapis Lazuli, NV · 2006 · cites it directly1descendant
- K161819NNR06 Multi-Purpose SolutionBausch & Lomb, Incorporated · 2016 · cites it directly0descendants
- K070767Eye See Multipurpose Contact Lens SolutionLapis Lazuli International NV · 2007 · 2 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K030092 | Complete Brand Multi-Purpose Solution | Advanced Medical Optics, Inc. | 2003 | — |
| +1 | K051104 | Eye See Multipurpose, NO-Rub Contact Lens Solution | Lapis Lazuli, NV | 2006 | — |
| +1 | K161819 | NNR06 Multi-Purpose Solution | Bausch & Lomb, Incorporated | 2016 | — |
| +2 | K070767 | Eye See Multipurpose Contact Lens Solution | Lapis Lazuli International NV | 2007 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2006 | 1 | 0 |
| 2007 | 1 | 0 |
| 2016 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), 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 K253795 MeniSept 3% Hydrogen Peroxide Cleaning &…score 12.7 · 4 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against?
The FDA summary names no predicate by number.
What descends from it? (3)
2 later devices cite it directly; ranked here by how many devices descend from each in turn.
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, K051104 (Lapis Lazuli, NV, 2006) has gone furthest, with 1 descendant of its own.
How does its category compare?
All LPN devicesLPN Accessories, Soft Lens Products: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · LPN
2in 2022
2026 to Oct 25, outlined.
Median 510(k) review, days · LPN
167in 2020
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · LPN
1in 2020
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · LPN
40in 2025
MAUDE reports naming product code LPN, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 4 | 175 | 2 | 1,151 |
| 2008 | 0 | — | 0 | 153 |
| 2009 | 1 | — | 2 | 121 |
| 2010 | 2 | — | 2 | 241 |
| 2011 | 3 | 222 | 1 | 273 |
| 2012 | 2 | — | 0 | 268 |
| 2013 | 2 | — | 0 | 84 |
| 2014 | 0 | — | 0 | 105 |
| 2015 | 2 | — | 0 | 176 |
| 2016 | 3 | 59 | 1 | 498 |
| 2017 | 1 | — | 0 | 2,666 |
| 2018 | 0 | — | 0 | 95 |
| 2019 | 2 | — | 0 | 60 |
| 2020 | 3 | 167 | 1 | 82 |
| 2021 | 2 | — | 0 | 51 |
| 2022 | 2 | — | 0 | 62 |
| 2023 | 0 | — | 0 | 84 |
| 2024 | 0 | — | 0 | 76 |
| 2025 | 0 | — | 0 | 40 |
| 2026 | 1 | — | 0 | — |
What is it indicated for?
COMPLETE@brand Multi-Purpose Solution is indicated for the care of soft (hydrophilic) contact lenses. Use this product, as recommended by your eye care practitioner, to:
Chemically (NOT HEAT) Disinfect
Clean
Rinse
Store
Remove Protein
Condition
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K030092 · printed Nov 6, 2026
Cite this page
510(k) Report. “K030092: Complete Brand Multi-Purpose Solution.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K030092
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026