510(k) · Cleared
ClearedPolaroid Contactspod
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Viopti, Ltd. · LRX Case, Contact Lens
Cleared on Feb 21, 2014 as substantially equivalent to K130753 (Watchdog Group, LC, 2013) after a 249-day review. Its family tree reaches back 4 generations to 1992.
- Decided
- Feb 21, 2014
- Review
- 249 days
- Class
- Class II
- Product code
- LRX
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 4 generations to K920064 (1992). 5 ancestors in all. No later device cites it as a predicate yet.
- Root · 4 generations backK920064 Opti-Lens Contact Lens CaseRyder Intl. Corp. · 1992
- 3 generations backK042578 I-Promotions Contact Lens CaseI-Promotions, Inc. · 2005
- 2 generations backK071081 Contact Lens CaseNingbo Kaida Rubber and Plastic Technology Co., LT · 2007
- 1 generation backK130753 Standard Contact Lens Case; Flip N Slide Contact Lens CaseWatchdog Group, LC · 2013
- This deviceK131783 Polaroid ContactspodViopti, Ltd. · 2014
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −4 | K920064 | Opti-Lens Contact Lens Case | Ryder Intl. Corp. | 1992 | — |
| −3 | K042578 | I-Promotions Contact Lens Case | I-Promotions, Inc. | 2005 | — |
| −2 | K071081 | Contact Lens Case | Ningbo Kaida Rubber and Plastic Technology Co., LT | 2007 | — |
| −1 | K130753 | Standard Contact Lens Case; Flip N Slide Contact Lens Case | Watchdog Group, LC | 2013 | — |
| 0 (this device) | K131783 | Polaroid Contactspod | Viopti, Ltd. | 2014 | — |
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 |
|---|---|---|---|
| * | K130753 | Standard Contact Lens Case; Flip N Slide Contact Lens CaseSummary page 2…on only. DO NOT USE WITH HEAT. Summary of Substantial Equivalence: The Viopti Device is substantially equivalent to WatchDog Group LC - Flip N Slide Contact Lens Case (K130753). The predicate device table has been prepared to compare the Contactspod with other medical devices already on the market… | 2013 |
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 22 years and passes through 5 companies; a new generation was cleared every 6.1 years on median.
- None of the 5 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. 2014, 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?
The Contactspod is a sterile single-use temporary storage case and contains multipurpose contact lens solution for use with soft contact lenses. It is not a replacement for your normal contact lens rub and rinse cleaning and disinfecting care regimen. It is a clear solution and should not be used if cloudy or discolored. Use for storage during chemical disinfection only. DO NOT USE WITH HEAT.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K131783 · printed Nov 5, 2026
Cite this page
510(k) Report. “K131783: Polaroid Contactspod.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K131783
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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