510(k) Report

510(k) · Cleared

Cleared

Motex Anti-Fog Surgical Face Mask

K201549510(k) TraditionalCleared Aug 26, 202078-day reviewClass II21 CFR 878.4040

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

Modern Healthcare Corp. · FXX Mask, Surgical

Cleared on Aug 26, 2020 as substantially equivalent to K063043 (Modern Healthcare Corp., 2007) after a 78-day review. Its family tree reaches back 4 generations to 1997. 1 later device descends from it.

Decided
Aug 26, 2020
Review
78 days
Class
Class II
Product code
FXX
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to K970835 (1997). 1 later device descends from it, 1 citing it directly.

  1. Root · 4 generations backK970835 Face Mask, Surgical Mask, Non-SterileTucker & Associates · 1997
  2. 3 generations backK022256 Surgical Face Mask - Colors: White, Yellow, Pink, Blue, and GreenTucker & Associates · 2004
  3. 2 generations backK060776 Surgical Face MaskHong YA Non-Woven Products Co., Ltd. · 2006
  4. 1 generation backK063043 Surgical Face Mask, Type: Tie-on, Ear-LoopModern Healthcare Corp. · 2007
  5. This deviceK201549 Motex Anti-Fog Surgical Face MaskModern Healthcare Corp. · 2020
  6. Descendant · cites it directly · 0 of its ownK212863 Surgical Face MaskTaiwan Comfort Champ Manufacturing Co., Ltd. · 2022

Most influential descendants

Showing 1 of 1 · See all
  • K212863Surgical Face MaskTaiwan Comfort Champ Manufacturing Co., Ltd. · 2022 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K970835Face Mask, Surgical Mask, Non-SterileTucker & Associates1997—
−3K022256Surgical Face Mask - Colors: White, Yellow, Pink, Blue, and GreenTucker & Associates2004—
−2K060776Surgical Face MaskHong YA Non-Woven Products Co., Ltd.2006—
−1K063043Surgical Face Mask, Type: Tie-on, Ear-LoopModern Healthcare Corp.2007—
0 (this device)K201549Motex Anti-Fog Surgical Face MaskModern Healthcare Corp.2020—
+1K212863Surgical Face MaskTaiwan Comfort Champ Manufacturing Co., Ltd.2022—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202210
FIG. 1 — Lineage of K201549, 1997–2022Source: 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 FXX? 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 FXX device

  1. #1 K201479 DemeMASKscore 40.2 · 6 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) 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.

TypeNumberDeviceApplicantDecidedRecalls
*K063043Surgical Face Mask, Type: Tie-on, Ear-Loop
Summary page 4
….4040 Surgical Mask Product Code: FXX Predicate Devices: Surgical Face Mask, type: Tie-on, Ear-loop K063043, Modern Healthcare Corp. Device Description: The Motex Anti-Fog Surgical Face Mask, type: Tie-on, Ear-loop, is flat pl…
Modern Healthcare Corp.2007—

Also cleared against K063043: 1 other device →

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K212863Surgical Face MaskTaiwan Comfort Champ Manufacturing Co., Ltd.20220

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 23 years and passes through 3 companies; a new generation was cleared every 6.6 years on median.
  • None of the 4 ancestors has a recall.
  • Of its descendants, K212863 (Taiwan Comfort Champ Manufacturing Co., Ltd., 2022) has gone furthest, with 0 descendants of its own.
  • 1 other device also cites its predicate K063043.

How does its category compare?

All FXX devices

FXX Mask, Surgical: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.

FDA decisions per year · FXX

6in 2025

2007: 22008: 22009: 12010: 72011: 62012: 12013: 32014: 12015: 52016: 52017: 12018: 32019: 42020: 272021: 2182022: 912023: 222024: 152025: 62026 (partial year): 5
2007high 218 (2021) · low 1 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FXX

123in 2025

2010: 144 days median2011: 137 days median2013: 219 days median2015: 298 days median2016: 268 days median2018: 119 days median2019: 124 days median2020: 113 days median2021: 162 days median2022: 113 days median2023: 139 days median2024: 263 days median2025: 123 days median2026 (partial year): 142 days median
2007high 298 (2015) · low 113 (2020)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · FXX

2in 2024

2019: 22023: 12024: 2
2007high 2 (2019) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · FXX

11in 2025

2007: 112008: 102009: 32010: 92011: 82012: 222013: 92014: 52015: 142016: 162017: 452018: 212019: 232020: 602021: 672022: 212023: 212024: 212025: 11
2007high 67 (2021) · low 3 (2009)2025

MAUDE reports naming product code FXX, 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
20072—011
20082—010
20091—03
2010714409
2011613708
20121—022
2013321909
20141—05
20155298014
20165268016
20171—045
20183119021
20194124223
202027113060
2021218162067
202291113021
202322139121
202415263221
20256123011
202651420—

What is it indicated for?

The Motex Anti-Fog Surgical Face Mask is intended to be worn to protect both the patient and healthcare personnel from transfer of microorganisms, body fluids, and particulate material. These face masks are intended for use in infection control practices to reduce potential exposure to blood and body fluids. The face mask is single use, disposable device, provided non-sterile.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K201549: Motex Anti-Fog Surgical Face Mask.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K201549

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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