510(k) Report

510(k) · Cleared

Cleared

Tuttnauer Pre-vacuum Steam Sterilizer models 3870HSG and 3870HSG-WS

K222608510(k) TraditionalCleared Dec 16, 2022109-day reviewClass II21 CFR 880.6880

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

Tuttnauer, Ltd. · FLE Sterilizer, Steam

Cleared on Dec 16, 2022 as substantially equivalent to K143311 (Tuttnauer U.S.A Co, Ltd., 2015) after a 109-day review. Its family tree reaches back 6 generations to 2001.

Decided
Dec 16, 2022
Review
109 days
Class
Class II
Product code
FLE
Recalls
None
Predicates
1

Its longest line of descent runs back 6 generations to K003470 (2001). 15 ancestors in all, the oldest K850264 (1985). No later device cites it as a predicate yet.

  1. Root · 6 generations backK003470 Ehs Series Table Top Autoclave, Models 2540 and 3870Tuttnauer Co., Ltd. · 2001
  2. 5 generations backK032192 Pre-Vacuum Autoclave with Steam Generator and Vertical Sliding Door…Tuttnauer U.S.A Co, Ltd. · 2004
  3. 4 generations backK063711 Tuttnauer Prevacuum Steam Heated Autoclave, Models 6990 SP-1A, 66120…Tuttnauer Co., Ltd. · 2007
  4. 3 generations backK090783 Tuttnauer Elara-11 Pre-Vacuum Tabletop AutoclaveTuttnauer U.S.A Co, Ltd. · 2009
  5. 2 generations backK111736 Tuttnauer EZ Plus Series Electronic Tabletop AutoclavesTuttnauer Co., Ltd. · 2011
  6. 1 generation backK143311 Pre-vacuum Tabletop AutoclaveTuttnauer U.S.A Co, Ltd. · 2015
  7. This deviceK222608 Tuttnauer Pre-vacuum Steam Sterilizer models 3870HSG and 3870HSG-WSTuttnauer, Ltd. · 2022
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K003470Ehs Series Table Top Autoclave, Models 2540 and 3870Tuttnauer Co., Ltd.2001—
−5K032192Pre-Vacuum Autoclave with Steam Generator and Vertical Sliding Door, Models…Tuttnauer U.S.A Co, Ltd.2004—
−4K063711Tuttnauer Prevacuum Steam Heated Autoclave, Models 6990 SP-1A, 66120 SP-1A…Tuttnauer Co., Ltd.2007—
−3K090783Tuttnauer Elara-11 Pre-Vacuum Tabletop AutoclaveTuttnauer U.S.A Co, Ltd.2009—
−2K111736Tuttnauer EZ Plus Series Electronic Tabletop AutoclavesTuttnauer Co., Ltd.2011—
−1K143311Pre-vacuum Tabletop AutoclaveTuttnauer U.S.A Co, Ltd.2015—
0 (this device)K222608Tuttnauer Pre-vacuum Steam Sterilizer models 3870HSG and 3870HSG-WSTuttnauer, Ltd.2022—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198510
199310
199410
199910
200110
200210
200320
200610
FIG. 1 — Lineage of K222608, 2001–2022Source: 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 FLE? 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 FLE device

  1. #1 K250168 Life Ultra 25L Tabletop Mono Chamber Steam…score 12.7 · 8 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
*K143311Pre-vacuum Tabletop Autoclave
Summary page 5
…Device class: II 3. PREDICATE DEVICES: • Tuttnauer pre-vacuum horizontal autoclave model 5075HSG, which was cleared under K143311. Product Code: FLE Regulation Number: 21CFR 880.6880 Page 1 of 11…
Tuttnauer U.S.A Co, Ltd.2015—

Also cleared against K143311: 2 other devices →

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 21 years and passes through 3 companies; a new generation was cleared every 3.1 years on median.
  • 1 of the 15 ancestors has a recall of any class.
  • 2 other devices also cite its predicate K143311.

How does its category compare?

All FLE devices

FLE Sterilizer, Steam: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, this device’s year, is highlighted.

FDA decisions per year · FLE

4in 2025

2007: 52008: 12009: 82010: 22011: 52012: 52013: 52014: 22015: 32016: 12017: 32018: 82019: 52020: 22021: 52022: 102023: 72024: 22025: 42026 (partial year): 3
2007high 10 (2022) · low 1 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FLE

184in 2025

2007: 67 days median2009: 109 days median2011: 141 days median2012: 111 days median2013: 241 days median2015: 302 days median2017: 233 days median2018: 146 days median2019: 192 days median2021: 147 days median2022: 133 days median2023: 88 days median2025: 184 days median2026 (partial year): 85 days median
2007high 302 (2015) · low 67 (2007)2026

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

Recalls per year · FLE

1in 2021

2007: 12008: 12011: 12012: 12013: 22015: 12018: 12019: 22021: 12026 (partial year): 1
2007high 2 (2013) · low 0 (2009)2026

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

Adverse event reports per year · FLE

71in 2025

2007: 192008: 212009: 192010: 202011: 632012: 692013: 1122014: 1132015: 682016: 762017: 632018: 902019: 912020: 872021: 812022: 702023: 662024: 642025: 71
2007high 113 (2014) · low 19 (2007)2025

MAUDE reports naming product code FLE, 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
2007567119
20081—121
20098109019
20102—020
20115141163
20125111169
201352412112
20142—0113
20153302168
20161—076
20173233063
20188146190
20195192291
20202—087
20215147181
202210133070
2023788066
20242—064
20254184071
20263851—

What is it indicated for?

The pre-vacuum steam sterilizer models 3870HSG and 3870HSG-WS are intended for use in hospitals and other health-

care facilities (e.g. hospitals, nursing homes, extended-care facilities, freestanding surgical centers, clinics, and medical

and dental offices) for the purpose of sterilizing heat stable medical devices: wrapped and unwrapped solids (IUSS), hollow and porous products.

The following table show the preprogrammed cycles, including sterilization temperature, sterilization time (in minutes), dry time (in minutes) and maximum load:

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K222608: Tuttnauer Pre-vacuum Steam Sterilizer models 3870HSG and 3870HSG-WS.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K222608

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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