510(k) Report

510(k) · Cleared

Cleared

Tecno-Gaz Andromeda Vacuum CS Autoclave

K063681510(k) TraditionalCleared Jun 29, 2007200-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

Mediline Italia S.R.L. · FLE Sterilizer, Steam

Cleared on Jun 29, 2007 as substantially equivalent to K023348 (Midmark Corp., 2003) and 2 other predicates after a 200-day review. Its family tree reaches back 3 generations to 1994.

Decided
Jun 29, 2007
Review
200 days
Class
Class II
Product code
FLE
Recalls
None
Predicates
3

Its longest line of descent runs back 3 generations to K936181 (1994). 7 ancestors in all, the oldest K900432 (1990). No later device cites it as a predicate yet.

Other ancestors, by year cleared 2001: 1 other ancestor1998: 1 other ancestor1991: 1 other ancestor1990: 1 other ancestorK936181 · Midmark M-11 Ultraclave Steam Sterilizer · Midmark Corp. · 1994 · recalledK990189 · Modification of: Midmark M-11 Ultraclave Steam Sterilizer · Midmark Corp. · 1999K023348 · Midmark M9 Ultraclave Steam Sterilizer · Midmark Corp. · 20031990199520002005
  1. Root · 3 generations backK936181 Midmark M-11 Ultraclave Steam SterilizerMidmark Corp. · 1994 · Recalled
  2. 2 generations backK990189 Modification of: Midmark M-11 Ultraclave Steam SterilizerMidmark Corp. · 1999
  3. 1 generation backK023348 Midmark M9 Ultraclave Steam SterilizerMidmark Corp. · 2003
  4. This deviceK063681 Tecno-Gaz Andromeda Vacuum CS AutoclaveMediline Italia S.R.L. · 2007
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K936181Midmark M-11 Ultraclave Steam SterilizerMidmark Corp.19941
−2K990189Modification of: Midmark M-11 Ultraclave Steam SterilizerMidmark Corp.1999—
−1K023348Midmark M9 Ultraclave Steam SterilizerMidmark Corp.2003—
0 (this device)K063681Tecno-Gaz Andromeda Vacuum CS AutoclaveMediline Italia S.R.L.2007—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199010
199110
199810
200110
FIG. 1 — Lineage of K063681, 1994–2007Source: 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? (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
*K023348Midmark M9 Ultraclave Steam Sterilizer
Summary page 1
…ces The Tecno-Gaz ANDROMEDA VACUUM CS Autoclave is substantially equivalent to the following devices: VMidmark M9 Ultraclave Steam Sterilizer (K023348), /Tuttnaucr EHS Series Table top autoclave (K003470) /Prestige Medical Series 2100Clinical Autoclave (K9…
Midmark Corp.2003—
*K003470Ehs Series Table Top Autoclave, Models 2540 and 3870
Summary page 1
…ntially equivalent to the following devices: VMidmark M9 Ultraclave Steam Sterilizer (K023348), /Tuttnaucr EHS Series Table top autoclave (K003470) /Prestige Medical Series 2100Clinical Autoclave (K962903)…
Tuttnauer Co., Ltd.2001—
*K962903Prestige Medical Series 2100 Clinical Autoclave
Summary page 1
…rk M9 Ultraclave Steam Sterilizer (K023348), /Tuttnaucr EHS Series Table top autoclave (K003470) /Prestige Medical Series 2100Clinical Autoclave (K962903) Page 4 of 38 oo00±)…
Prestige Medical Corp.1998—

Also cleared against K023348: 3 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 13 years and passes through 2 companies; a new generation was cleared every 4.3 years on median.
  • 1 of the 7 ancestors has a recall of any class.
  • 3 other devices also cite its predicate K023348.

How does its category compare?

All FLE devices

FLE Sterilizer, Steam: FDA decisions, review times, recalls and adverse event reports over 20 years. 2007, 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?

Tecno-Gaz ANDROMEDA VACUUM CS Autoclave is intended to be used in medical and dental offices, hospitals, clinics, nursing homes, and other facilities to sterilize heat and moisture-stable, reusable items (including dental hand pieces) that are compatible with steam sterilization. Refer to Standard Cycle Parameters for detailed information.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K063681: Tecno-Gaz Andromeda Vacuum CS Autoclave.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K063681

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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