510(k) Report

510(k) · Cleared

Cleared

Hoffrichter Trend 110 Cpap Device with Aquatrend Iii Cpap Humidifier Accessory for Trend

K041035510(k) TraditionalCleared Jun 9, 200449-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

Hoffrichter GmbH · BZD Ventilator, Non-Continuous (Respirator)

Cleared on Jun 9, 2004 as substantially equivalent to K014074 (Hoffrichter GmbH, 2003) and 2 other predicates after a 49-day review. Its family tree reaches back 4 generations to 1995. 1 later device descends from it.

Decided
Jun 9, 2004
Review
49 days
Class
Class II
Product code
BZD
Recalls
None
Predicates
3

Its longest line of descent runs back 4 generations to K952292 (1995). 8 ancestors in all, the oldest K915460 (1993). 1 later device descends from it, 1 citing it directly.

  1. Root · 4 generations backK952292 Puritan-Bennett Companion Nasal Cpap SystemPuritan Bennett Corp. · 1995
  2. 3 generations backK961626 Solo Cpap SystemRespironics, Inc. · 1996
  3. 2 generations backK973161 Cpap Humidifier (HC 200)Fisher & Paykel Electronics, Ltd. · 1998
  4. 1 generation backK014074 Hoffrichter Vector, Vector Plus, Vector BI-Vevel, Vector BI-Level…Hoffrichter GmbH · 2003
  5. This deviceK041035 Hoffrichter Trend 110 Cpap Device with Aquatrend Iii Cpap Humidifier…Hoffrichter GmbH · 2004
  6. Descendant · cites it directly · 0 of its ownK053486 Trend 200 Cpap Device, Model 5CP201; Trendset PC Software, Model…Hoffrichter GmbH · 2006

Most influential descendants

Showing 1 of 1 · See all
  • K053486Trend 200 Cpap Device, Model 5CP201; Trendset PC Software, Model TrendsetHoffrichter GmbH · 2006 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K952292Puritan-Bennett Companion Nasal Cpap SystemPuritan Bennett Corp.1995—
−3K961626Solo Cpap SystemRespironics, Inc.1996—
−2K973161Cpap Humidifier (HC 200)Fisher & Paykel Electronics, Ltd.1998—
−1K014074Hoffrichter Vector, Vector Plus, Vector BI-Vevel, Vector BI-Level Plus…Hoffrichter GmbH2003—
0 (this device)K041035Hoffrichter Trend 110 Cpap Device with Aquatrend Iii Cpap Humidifier Accessory…Hoffrichter GmbH2004—
+1K053486Trend 200 Cpap Device, Model 5CP201; Trendset PC Software, Model TrendsetHoffrichter GmbH2006—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199310
199410
199610
200110

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200610
FIG. 1 — Lineage of K041035, 1995–2006Source: 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 BZD? 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 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
Get a 510(k) Report

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
*K014074Hoffrichter Vector, Vector Plus, Vector BI-Vevel, Vector BI-Level Plus, Scalar, Scalar…
Summary page 1
…Class II (3) Predicate Device(s): · SCALAR/VECTOR CPAP with Humidifier 'Plus" option (K014074) * Fischer and Paykel HC200 CPAP…
Hoffrichter GmbH2003—
*K973161Cpap Humidifier (HC 200)
Summary page 1
…option (K014074) * Fischer and Paykel HC200 CPAP with Heated Humidifier (K973161) * Invacare Poseidon Passover Hum…
Fisher & Paykel Electronics, Ltd.1998—
*K003561Invacare Passover Humidifier Model ISP9700
Summary page 1
…with Heated Humidifier (K973161) * Invacare Poseidon Passover Humidifier (K003561) Reason for Submission: New Device (4) Description of Device: Hoffrichter TR…
Invacare Corp.2001—

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K053486Trend 200 Cpap Device, Model 5CP201; Trendset PC Software, Model TrendsetHoffrichter GmbH20060

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 9 years and passes through 4 companies; a new generation was cleared every 2.0 years on median.
  • None of the 8 ancestors has a recall.
  • Of its descendants, K053486 (Hoffrichter GmbH, 2006) 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.

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 TREND 110 device is for treatment of obstructive sleep apnea (OSA) in adult patients weighing at least 30 kg. These devices are not intended for use with ventilator-dependent patients.

The TREND 110 device provides continuous positive airway pressure.

The AquaTREND Humidifier accessory provides humidification of the air delivered to the patient.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K041035: Hoffrichter Trend 110 Cpap Device with Aquatrend Iii Cpap Humidifier Accessory for Trend.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K041035

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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