510(k) Report

510(k) · Cleared

Cleared

Soft Grip Contact Lens Case, Deluxe Contact Lens Case, Econo-Mate Contact Lens Case

K111856510(k) TraditionalCleared Jul 14, 201115-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

Apothecary Products, Inc. · LRX Case, Contact Lens

Cleared on Jul 14, 2011 as substantially equivalent to K093377 (Reliance Design & Manufacturing Corp., 2010) and 2 other predicates after a 15-day review. Its family tree reaches back 4 generations to 1992.

Decided
Jul 14, 2011
Review
15 days
Class
Class II
Product code
LRX
Recalls
None
Predicates
3

Its longest line of descent runs back 4 generations to K920064 (1992). 6 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 4 generations backK920064 Opti-Lens Contact Lens CaseRyder Intl. Corp. · 1992
  2. 3 generations backK042578 I-Promotions Contact Lens CaseI-Promotions, Inc. · 2005
  3. 2 generations backK071081 Contact Lens CaseNingbo Kaida Rubber and Plastic Technology Co., LT · 2007
  4. 1 generation backK093377 Polaris Contact Lens CaseReliance Design & Manufacturing Corp. · 2010
  5. This deviceK111856 Soft Grip Contact Lens Case, Deluxe Contact Lens Case, Econo-Mate…Apothecary Products, Inc. · 2011
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K920064Opti-Lens Contact Lens CaseRyder Intl. Corp.1992—
−3K042578I-Promotions Contact Lens CaseI-Promotions, Inc.2005—
−2K071081Contact Lens CaseNingbo Kaida Rubber and Plastic Technology Co., LT2007—
−1K093377Polaris Contact Lens CaseReliance Design & Manufacturing Corp.2010—
0 (this device)K111856Soft Grip Contact Lens Case, Deluxe Contact Lens Case, Econo-Mate Contact Lens…Apothecary Products, Inc.2011—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200010
200310
FIG. 1 — Lineage of K111856, 1992–2011Source: 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 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. #1 K240095 CAREUS Contact Lens Case (Model 1, Model 2…score 15.3 · 5 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (3)

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.

TypeNumberDeviceApplicantDecidedRecalls
*K093377Polaris Contact Lens Case
Summary page 1
…Common or usual name: Contact Lens Case Classification: Class 11, 21 CER 886.5928 Product Code: LRX Predicate Device information: K093377; K991 206; K042578 Device Description: The API Soft Grip Contact Lens Cases and Deluxe…
Reliance Design & Manufacturing Corp.2010—
*K991206Bonasse Contact Lens Case
Summary page 1
…usual name: Contact Lens Case Classification: Class 11, 21 CER 886.5928 Product Code: LRX Predicate Device information: K093377; K991 206; K042578 Device Description: The API Soft Grip Contact Lens Cases and Deluxe Contact L…
Bonasse Ent. Co., Ltd.2000—
*K042578I-Promotions Contact Lens Case
Summary page 1
…e: Contact Lens Case Classification: Class 11, 21 CER 886.5928 Product Code: LRX Predicate Device information: K093377; K991 206; K042578 Device Description: The API Soft Grip Contact Lens Cases and Deluxe Contact Lens Cases…
I-Promotions, Inc.2005—

Also cleared against K093377: 1 other device →

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 19 years and passes through 5 companies; a new generation was cleared every 3.0 years on median.
  • None of the 6 ancestors has a recall.
  • 1 other device also cites its predicate K093377.

How does its category compare?

All LRX devices

LRX Case, Contact Lens: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.

FDA decisions per year · LRX

1in 2025

2007: 12009: 12010: 12011: 22012: 32013: 42014: 32015: 22016: 22017: 52023: 12024: 12025: 12026 (partial year): 1
2007high 5 (2017) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LRX

49in 2017

2012: 103 days median2013: 72 days median2014: 249 days median2017: 49 days median
2007high 249 (2014) · low 49 (2017)2026

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

2012: 12014: 12017: 32021: 1
2007high 3 (2017) · low 0 (2007)2025

MAUDE reports naming product code LRX, 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
20071—00
20080—00
20091—00
20101—00
20112—00
2012310301
201347200
2014324901
20152—00
20162—00
201754903
20180—00
20190—00
20200—00
20210—01
20220—00
20231—00
20241—00
20251—00
20261—0—

What is it indicated for?

The API Soft Grip, 68012, 68013; Deluxe, K1020; and Econo-Mate, K1010 Contact Lens Cases are intended for the storage of soft (hydrophilic), rigid gas permeable (RGP), or hard contact lenses during chemical disinfection. For use in storage during chemical disinfection only. Do not use during heat disinfection.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K111856: Soft Grip Contact Lens Case, Deluxe Contact Lens Case, Econo-Mate Contact Lens Case.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K111856

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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