510(k) Report

510(k) · Cleared

Cleared

Soyala Full Face Mask Gel Vented

K073673510(k) SpecialCleared Mar 28, 200892-day reviewClass II21 CFR 868.5905

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

Weinmann Gerate Fur Medizin GmbH + Co. KG · BZD Ventilator, Non-Continuous (Respirator)

Cleared on Mar 28, 2008 as substantially equivalent to K061653 (Weinmann Gerate Fur Medizin GmbH + Co. KG, 2006) after a 92-day review. Its family tree reaches back 5 generations to 1983. 1 later device descends from it.

Decided
Mar 28, 2008
Review
92 days
Class
Class II
Product code
BZD
Recalls
None
Predicates
1

Its longest line of descent runs back 5 generations to K833786 (1983). 15 ancestors in all. 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2006: 1 other ancestor2004: 2 other ancestors2002: 1 other ancestor2000: 1 other ancestor1999: 1 other ancestor1998: 1 other ancestor2003: 1 other ancestor2001: 1 other ancestor1988: 1 other ancestor2011: 1 descendant clearedK833786 · Microprocessor Ventilator 7200 · Puritan Bennett Corp. · 1983K951264 · Bipap Model S/T-D · Respironics, Inc. · 1996K991648 · Reusable Contour II Nasal Mask · Respironics, Inc. · 1999K013738 · Weinmann Somnomask · Gottlieb Weinmann Geraete Fuer Medizin Und Arbeits · 2002K061653 · Soyala Full Face Mask · Weinmann Gerate Fur Medizin GmbH + Co. KG · 200619801990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 3 other ancestors3 generations back: 4 other ancestors4 generations back: 1 other ancestor5 generations back: 2 other ancestors 1 generation forward: 1 descendant K061653 · Soyala Full Face Mask · Weinmann Gerate Fur Medizin GmbH + Co. KG · 2006K013738 · Weinmann Somnomask · Gottlieb Weinmann Geraete Fuer Medizin Und Arbeits · 2002K991648 · Reusable Contour II Nasal Mask · Respironics, Inc. · 1999K951264 · Bipap Model S/T-D · Respironics, Inc. · 1996K833786 · Microprocessor Ventilator 7200 · Puritan Bennett Corp. · 1983−50
  1. Root · 5 generations backK833786 Microprocessor Ventilator 7200Puritan Bennett Corp. · 1983
  2. 4 generations backK951264 Bipap Model S/T-DRespironics, Inc. · 1996
  3. 3 generations backK991648 Reusable Contour II Nasal MaskRespironics, Inc. · 1999
  4. 2 generations backK013738 Weinmann SomnomaskGottlieb Weinmann Geraete Fuer Medizin Und Arbeits · 2002
  5. 1 generation backK061653 Soyala Full Face MaskWeinmann Gerate Fur Medizin GmbH + Co. KG · 2006
  6. This deviceK073673 Soyala Full Face Mask Gel VentedWeinmann Gerate Fur Medizin GmbH + Co. KG · 2008
  7. Descendant · cites it directly · 0 of its ownK112167 Soyala Silkgel Full Face MaskWeinmann Gerate Fur Medizin GmbH + Co. KG · 2011

Most influential descendants

Showing 1 of 1 · See all
  • K112167Soyala Silkgel Full Face MaskWeinmann Gerate Fur Medizin GmbH + Co. KG · 2011 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K833786Microprocessor Ventilator 7200Puritan Bennett Corp.1983—
−4K951264Bipap Model S/T-DRespironics, Inc.1996—
−3K991648Reusable Contour II Nasal MaskRespironics, Inc.1999—
−2K013738Weinmann SomnomaskGottlieb Weinmann Geraete Fuer Medizin Und Arbeits2002—
−1K061653Soyala Full Face MaskWeinmann Gerate Fur Medizin GmbH + Co. KG2006—
0 (this device)K073673Soyala Full Face Mask Gel VentedWeinmann Gerate Fur Medizin GmbH + Co. KG2008—
+1K112167Soyala Silkgel Full Face MaskWeinmann Gerate Fur Medizin GmbH + Co. KG2011—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198810
199810
199910
200010
200110
200210
200310
200420
200610

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201110
FIG. 1 — Lineage of K073673, 1983–2011Source: 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.

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Top candidate predicates for a new BZD device

  1. #1 K250624 myAirscore 15.7 · 12 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? (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
*K061653Soyala Full Face Mask
Summary page 1
…68.5905, Class II,Product Code BZD Predicate Device Equivalence: Substantial equivalence is claimed to SOYALA Full Face Mask, cleared for commercial distribution per K061653. Device Description: The SOYALA Full Face Mask GEL vented is a molded plastic mask, including an exhalation system, for the…
Weinmann Gerate Fur Medizin GmbH + Co. KG2006—

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K112167Soyala Silkgel Full Face MaskWeinmann Gerate Fur Medizin GmbH + Co. KG20110

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 25 years and passes through 4 companies; a new generation was cleared every 2.8 years on median.
  • 3 of the 15 ancestors have a recall of any class.
  • Of its descendants, K112167 (Weinmann Gerate Fur Medizin GmbH + Co. KG, 2011) has gone furthest, with 0 descendants of its own.

How does its category compare?

All BZD devices

BZD Ventilator, Non-Continuous (Respirator): FDA decisions, review times, recalls and adverse event reports over 20 years. 2008, this device’s year, is highlighted.

FDA decisions per year · BZD

7in 2025

2007: 212008: 172009: 232010: 122011: 232012: 212013: 232014: 142015: 112016: 122017: 52018: 52019: 62020: 62021: 62022: 42023: 52024: 102025: 72026 (partial year): 10
2007high 23 (2009) · low 4 (2022)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · BZD

189in 2025

2007: 83 days median2008: 108 days median2009: 90 days median2010: 122 days median2011: 125 days median2012: 133 days median2013: 127 days median2014: 172 days median2015: 224 days median2016: 217 days median2017: 221 days median2018: 280 days median2019: 231 days median2020: 137 days median2021: 192 days median2022: 253 days median2023: 204 days median2024: 132 days median2025: 189 days median2026 (partial year): 214 days median
2007high 280 (2018) · low 83 (2007)2026

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

Recalls per year · BZD

8in 2023

2007: 292008: 22009: 12011: 12019: 4, 4 Class I2023: 8, 7 Class I2026 (partial year): 2, 2 Class I
2007high 29 (2007) · low 0 (2010)2026

Class I (13 since 2007) Class II/III not classified

Adverse event reports per year · BZD

60,279in 2025

2007: 652008: 672009: 1472010: 1432011: 1892012: 1392013: 822014: 862015: 1142016: 1182017: 1482018: 1012019: 1882020: 1262021: 6,0662022: 90,7682023: 27,9872024: 68,2622025: 60,279
2007high 90,768 (2022) · low 65 (2007)2025

MAUDE reports naming product code BZD, 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
200721832965
200817108267
200923901147
2010121220143
2011231251189
2012211330139
201323127082
201414172086
2015112240114
2016122170118
201752210148
201852800101
201962314 (4)188
202061370126
2021619206,066
20224253090,768
202352048 (7)27,987
202410132068,262
20257189060,279
2026102142 (2)—

What is it indicated for?

The Full Face Mask is intended for adult patients (>30kg) prescribed continuous positive airway pressure (CPAP) or bi-level therapy for multiple patient use in a hospital or clinic environment after high-level disinfection and for single-patient use in a home environment.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K073673: Soyala Full Face Mask Gel Vented.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K073673

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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