510(k) · Cleared
Cleared3M Vflex Health Care Particulate Respirator and Surgical Mask
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
3M Company · MSH Respirator, Surgical
Cleared on Feb 11, 2013 as substantially equivalent to K063023 (3M Company, 2007) after a 308-day review. Its family tree reaches back 1 generation to 2007. 3 later devices descend from it.
- Decided
- Feb 11, 2013
- Review
- 308 days
- Class
- Class II
- Product code
- MSH
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to K063023 (2007). 3 later devices descend from it, 1 citing it directly.
- Root · 1 generation backK063023 3M Health Care Particulate Respirator and Surgical Mask, Model 18703M Company · 2007
- This deviceK121069 3M Vflex Health Care Particulate Respirator and Surgical Mask3M Company · 2013
- Descendant · cites it directly · 2 of its ownK172500 Technoweb Surgical MaskYts Global, Inc. · 2018
- Descendant · 2 generations on · 0 of its ownK243342 KP Protective Face MaskKp Trading Co., Ltd. · 2025
- Descendant · 2 generations on · 0 of its ownK223270 POSE™ Health Care Surgical MaskAmerica'S Supply Chains · 2022
Most influential descendants
Showing 3 of 3 · See allView FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K063023 | 3M Health Care Particulate Respirator and Surgical Mask, Model 1870 | 3M Company | 2007 | — |
| 0 (this device) | K121069 | 3M Vflex Health Care Particulate Respirator and Surgical Mask | 3M Company | 2013 | — |
| +1 | K172500 | Technoweb Surgical Mask | Yts Global, Inc. | 2018 | — |
| +2 | K243342 | KP Protective Face Mask | Kp Trading Co., Ltd. | 2025 | — |
| +2 | K223270 | POSE™ Health Care Surgical Mask | America'S Supply Chains | 2022 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2018 | 1 | 0 |
| 2022 | 1 | 0 |
| 2025 | 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 MSH? 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 MSH device
- #1 K233022 Halyard Fluidshield 3 N95 Particulate Filter…score 6.7 · 1 generation · no Class I recall
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 |
|---|---|---|---|
| * | K063023 | 3M Health Care Particulate Respirator and Surgical Mask, Model 1870Summary page 2…Care Particulate and Surgical Mask, Respirator and Surgical Model 1570 (K063023) Mask, Model ____ ______ ___ ___ ____ ___ ___ ___… | 2007 |
What descends from it? (3)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K172500 | Technoweb Surgical Mask | 2018 | 2 |
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?
How does its category compare?
All MSH devicesMSH Respirator, Surgical: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.
FDA decisions per year · MSH
1in 2024
2026 to Oct 25, outlined.
Median 510(k) review, days · MSH
60in 2010
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · MSH
1in 2008
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · MSH
10in 2025
MAUDE reports naming product code MSH, 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 | 7 | 78 | 0 | 0 |
| 2008 | 2 | — | 1 | 0 |
| 2009 | 2 | — | 0 | 0 |
| 2010 | 4 | 60 | 0 | 2 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 1 | — | 0 | 0 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 1 | — | 0 | 3 |
| 2016 | 1 | — | 0 | 0 |
| 2017 | 1 | — | 0 | 2 |
| 2018 | 1 | — | 0 | 4 |
| 2019 | 0 | — | 0 | 0 |
| 2020 | 0 | — | 0 | 59 |
| 2021 | 0 | — | 0 | 19 |
| 2022 | 0 | — | 0 | 18 |
| 2023 | 0 | — | 0 | 71 |
| 2024 | 1 | — | 0 | 1 |
| 2025 | 0 | — | 0 | 10 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
3M™ VFlex™ Health Care Particulate Respirator and Surgical Mask 1805/1805S is intended to be worn by operating room personnel during surgical procedures to protect both the surgical patient and the operating room personnel from transfer of microorganisms, body fluids, and particulate material.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K121069 · printed Nov 6, 2026
Cite this page
510(k) Report. “K121069: 3M Vflex Health Care Particulate Respirator and Surgical Mask.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K121069
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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