510(k) · Cleared
ClearedMenicon Nect Contact Lens Case
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Foresight Regulatory Strategies · LRX Case, Contact Lens
Cleared on Aug 6, 2013 as substantially equivalent to K121030 (Sacks Holdings, Inc., 2012) after a 43-day review. Its family tree reaches back 3 generations to 1992.
- Decided
- Aug 6, 2013
- Review
- 43 days
- Class
- Class II
- Product code
- LRX
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 3 generations to K920064 (1992). 4 ancestors in all. No later device cites it as a predicate yet.
- Root · 3 generations backK920064 Opti-Lens Contact Lens CaseRyder Intl. Corp. · 1992
- 2 generations backK042578 I-Promotions Contact Lens CaseI-Promotions, Inc. · 2005
- 1 generation backK121030 Sacks Holdings Inc.'S Contact Lens Storage CaseSacks Holdings, Inc. · 2012
- This deviceK131875 Menicon Nect Contact Lens CaseForesight Regulatory Strategies · 2013
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −3 | K920064 | Opti-Lens Contact Lens Case | Ryder Intl. Corp. | 1992 | — |
| −2 | K042578 | I-Promotions Contact Lens Case | I-Promotions, Inc. | 2005 | — |
| −1 | K121030 | Sacks Holdings Inc.'S Contact Lens Storage Case | Sacks Holdings, Inc. | 2012 | — |
| 0 (this device) | K131875 | Menicon Nect Contact Lens Case | Foresight Regulatory Strategies | 2013 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2003 | 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 LRX? 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 LRX device
- #1 K240095 CAREUS Contact Lens Case (Model 1, Model 2…score 15.3 · 5 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (1)
Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K121030 | Sacks Holdings Inc.'S Contact Lens Storage CaseSummary page 1…Product code: LRX Proprietary name: Menicon Nect Contact Lens Case 3. Predicate Devices Menicon Nect claims substantial equivalence to K121030 Sacks Holdings, Inc. Contact Lens Storage Case cleared by the Food and Drug Administration on July 6, 2012. 4. Description o… | 2012 |
What descends from it?
No later submission names this one as a predicate yet.
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?
- The line of descent spans 21 years and passes through 4 companies; a new generation was cleared every 7.4 years on median.
- None of the 4 ancestors has a recall.
How does its category compare?
All LRX devicesLRX Case, Contact Lens: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.
FDA decisions per year · LRX
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · LRX
49in 2017
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · LRX
No recall names LRX since 2007.
Adverse event reports per year · LRX
1in 2021
MAUDE reports naming product code LRX, 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 | 1 | — | 0 | 0 |
| 2008 | 0 | — | 0 | 0 |
| 2009 | 1 | — | 0 | 0 |
| 2010 | 1 | — | 0 | 0 |
| 2011 | 2 | — | 0 | 0 |
| 2012 | 3 | 103 | 0 | 1 |
| 2013 | 4 | 72 | 0 | 0 |
| 2014 | 3 | 249 | 0 | 1 |
| 2015 | 2 | — | 0 | 0 |
| 2016 | 2 | — | 0 | 0 |
| 2017 | 5 | 49 | 0 | 3 |
| 2018 | 0 | — | 0 | 0 |
| 2019 | 0 | — | 0 | 0 |
| 2020 | 0 | — | 0 | 0 |
| 2021 | 0 | — | 0 | 1 |
| 2022 | 0 | — | 0 | 0 |
| 2023 | 1 | — | 0 | 0 |
| 2024 | 1 | — | 0 | 0 |
| 2025 | 1 | — | 0 | 0 |
| 2026 | 1 | — | 0 | — |
What is it indicated for?
Menicon Nect Contact Lens Case is indicated for storage during chemical disinfection of soft (hydrophilic), rigid gas permeable and hard contact lenses. This case is for use during chemical disinfection only. Not to be used with heat disinfection.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K131875 · printed Nov 5, 2026
Cite this page
510(k) Report. “K131875: Menicon Nect Contact Lens Case.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K131875
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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