510(k) Report

510(k) · Cleared

Cleared

AllerBlock Junior

K201734510(k) TraditionalCleared Mar 26, 2021274-day reviewClass II21 CFR 880.5045

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

Nasaleze International, Ltd. · NUP Cream, Nasal, Topical, Mechanical Allergen Particle Barrier

Cleared on Mar 26, 2021 as substantially equivalent to K170848 (Nasaleze International, Ltd., 2017) after a 274-day review. Its family tree reaches back 7 generations to 2001.

Decided
Mar 26, 2021
Review
274 days
Class
Class II
Product code
NUP
Recalls
None
Predicates
1

Its longest line of descent runs back 7 generations to K002338 (2001). 9 ancestors in all, the oldest K872359 (1987). No later device cites it as a predicate yet.

  1. Root · 7 generations backK002338 Liquiderm Liquid Adhesive BandageClosure Medical Corp. · 2001
  2. 6 generations backK022645 CURADBeiersdorf AG · 2002
  3. 5 generations backK032948 Elastic Skin Liquid BandageMedpak, LLC · 2004
  4. 4 generations backK042610 DR. Theiss Alergol Pollen Blocker CreamDr. Theiss Naturwaren GmbH · 2005
  5. 3 generations backK053625 NasalguardTrutek Corp · 2006
  6. 2 generations backK132520 Nasal Ease Allergy BlockerHi-Tech Pharmacal, Inc. · 2013
  7. 1 generation backK170848 Alzair Allergy BlockerNasaleze International, Ltd. · 2017
  8. This deviceK201734 AllerBlock JuniorNasaleze International, Ltd. · 2021
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K002338Liquiderm Liquid Adhesive BandageClosure Medical Corp.2001—
−6K022645CURADBeiersdorf AG2002—
−5K032948Elastic Skin Liquid BandageMedpak, LLC2004—
−4K042610DR. Theiss Alergol Pollen Blocker CreamDr. Theiss Naturwaren GmbH2005—
−3K053625NasalguardTrutek Corp2006—
−2K132520Nasal Ease Allergy BlockerHi-Tech Pharmacal, Inc.2013—
−1K170848Alzair Allergy BlockerNasaleze International, Ltd.2017—
0 (this device)K201734AllerBlock JuniorNasaleze International, Ltd.2021—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198710
199810
FIG. 1 — Lineage of K201734, 2001–2021Source: 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 NUP? 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 NUP device

  1. #1 K213114 BentrioTM Allergy Blockerscore 5.1 · 6 generations · no Class I recall
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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.

TypeNumberDeviceApplicantDecidedRecalls
*K170848Alzair Allergy Blocker
Summary page 4
…Name: Topical Nasal Cream -- Mechanical Allergen Particle Barrier Regulation 21 CRF 880.5045 / NUP / Class II Predicate Device K170848 Alzair Allergy Blocker Cleared 06-14-17 Basis for Submission 1. Expanded the Indications for Use to include pediatric patients (8…
Nasaleze International, Ltd.2017—

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 20 years and passes through 7 companies; a new generation was cleared every 1.8 years on median.
  • None of the 9 ancestors has a recall.

How does its category compare?

All NUP devices

NUP Cream, Nasal, Topical, Mechanical Allergen Particle Barrier: FDA decisions, review times, recalls and adverse event reports over 20 years. 2021, this device’s year, is highlighted.

FDA decisions per year · NUP

1in 2022

2012: 12013: 12014: 12017: 12021: 12022: 1
2007high 1 (2012) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NUP

Too few NUP 510(k)s in any year since 2007 to give a median.

Recalls per year · NUP

No recall names NUP since 2007.

Adverse event reports per year · NUP

1in 2024

2020: 12024: 1
2007high 1 (2020) · low 0 (2007)2025

MAUDE reports naming product code NUP, 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
20070—00
20080—00
20090—00
20100—00
20110—00
20121—00
20131—00
20141—00
20150—00
20160—00
20171—00
20180—00
20190—00
20200—01
20211—00
20221—00
20230—00
20240—01
20250—00
20260—0—

What is it indicated for?

AllerBlock Junior is intended for use in adults and children (8 years or older) to treat hay fever and allergy sufferers by

promoting alleviation of mild allergic symptoms (i.e., mild nasal irritation including itchy, runny, or congested nasal passages) triggered by the inhalation of various airborne allergens including indoor and outdoor environmental pollens, house dust, animal hairs, and dust mites.

Application of AllerBlock Junior produces a mucous-like gel barrier that evenly coats the nasal membranes and acts to block inhaled allergens within the nasal cavity.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K201734: AllerBlock Junior.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K201734

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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