510(k) Report

510(k) · Cleared

Cleared

V-Pro Sterilization Tray/ Sterilization Mat

K140494510(k) TraditionalCleared Jul 25, 2014148-day reviewClass II21 CFR 880.6850

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

STERIS Corporation · KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

Cleared on Jul 25, 2014 as substantially equivalent to K070769 (STERIS Corporation, 2007) and 1 other predicate after a 148-day review. Its family tree reaches back 7 generations to 1984. 7 later devices descend from it.

Decided
Jul 25, 2014
Review
148 days
Class
Class II
Product code
KCT
Recalls
None
Predicates
2

Its longest line of descent runs back 7 generations to K844002 (1984). 13 ancestors in all. 7 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2011: 1 other ancestor2004: 1 other ancestor2002: 1 other ancestor2001: 1 other ancestor1994: 1 other ancestor1997: 1 other ancestor2016: 1 descendant cleared2018: 1 descendant cleared2019: 2 descendants cleared2022: 1 descendant cleared2023: 2 descendants clearedK844002 · HU-Friedy Ims Cassette System · Hu-Friedy Mfg. Co., Inc. · 1984K980065 · C/T Med-Systems Cassette System · C/T Med System, Ltd. · 1998K990761 · Tuttnauer Mini Container Cassette, Tuttnauer Standard Case Cassette · Tuttnauer U.S.A Co, Ltd. · 1999K012105 · Polyvac Surgical Instrument Delivery System · Symmetry Medical, Inc. · 2002K023658 · Sterilization Cases and Trays · Carr Metal Products, Inc. · 2003K052992 · Conmed Linvatec Instrument Sterilization Tray · Conmed Linvatec · 2006K070769 · VHP 136 Tray · STERIS Corporation · 200719801990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor2 generations back: 2 other ancestors3 generations back: 2 other ancestors5 generations back: 1 other ancestor 1 generation forward: 1 descendant2 generations forward: 1 descendant3 generations forward: 2 descendants4 generations forward: 1 descendant5 generations forward: 2 descendants K070769 · VHP 136 Tray · STERIS Corporation · 2007K052992 · Conmed Linvatec Instrument Sterilization Tray · Conmed Linvatec · 2006K023658 · Sterilization Cases and Trays · Carr Metal Products, Inc. · 2003K012105 · Polyvac Surgical Instrument Delivery System · Symmetry Medical, Inc. · 2002K990761 · Tuttnauer Mini Container Cassette, Tuttnauer Standard Case Cassette · Tuttnauer U.S.A Co, Ltd. · 1999K980065 · C/T Med-Systems Cassette System · C/T Med System, Ltd. · 1998K844002 · HU-Friedy Ims Cassette System · Hu-Friedy Mfg. Co., Inc. · 1984−50+5
  1. Root · 7 generations backK844002 HU-Friedy Ims Cassette SystemHu-Friedy Mfg. Co., Inc. · 1984
  2. 6 generations backK980065 C/T Med-Systems Cassette SystemC/T Med System, Ltd. · 1998
  3. 5 generations backK990761 Tuttnauer Mini Container Cassette, Tuttnauer Standard Case CassetteTuttnauer U.S.A Co, Ltd. · 1999
  4. 4 generations backK012105 Polyvac Surgical Instrument Delivery SystemSymmetry Medical, Inc. · 2002
  5. 3 generations backK023658 Sterilization Cases and TraysCarr Metal Products, Inc. · 2003
  6. 2 generations backK052992 Conmed Linvatec Instrument Sterilization TrayConmed Linvatec · 2006
  7. 1 generation backK070769 VHP 136 TraySTERIS Corporation · 2007
  8. This deviceK140494 V-Pro Sterilization Tray/ Sterilization MatSTERIS Corporation · 2014
  9. Descendant · cites it directly · 6 of its ownK160912 Sterilization TraySTERIS Corporation · 2016
  10. Descendant · 2 generations on · 5 of its ownK172755 PRO-LITE Sterilization TraysSTERIS Corporation · 2018
  11. Descendant · 3 generations on · 3 of its ownK183402 PRO-LITE Sterilization TraySTERIS Corporation · 2019
  12. Descendant · 4 generations on · 2 of its ownK222440 Vis-U-All Low Temperature Sterilization Pouches/Tubing, PRO-LITE…Steris · 2022
  13. Descendant · 5 generations on · 0 of its ownK231501 PRO-LITE Sterilization TraySTERIS Corporation · 2023

Showing 5 of 7 descendants. See all descendants

Descendants cleared per year

2016: 12018: 12019: 22022: 12023: 2
2016high 2 (2019) · low 0 (2017)2026

Most influential descendants

Showing 5 of 7 · See all
  • K160912Sterilization TraySTERIS Corporation · 2016 · cites it directly6descendants
  • K172755PRO-LITE Sterilization TraysSTERIS Corporation · 2018 · 2 generations on5descendants
  • K183402PRO-LITE Sterilization TraySTERIS Corporation · 2019 · 3 generations on3descendants
  • K222440Vis-U-All Low Temperature Sterilization Pouches/Tubing, PRO-LITE Sterilization TraysSteris · 2022 · 4 generations on2descendants
  • K231501PRO-LITE Sterilization TraySTERIS Corporation · 2023 · 5 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K844002HU-Friedy Ims Cassette SystemHu-Friedy Mfg. Co., Inc.1984—
−6K980065C/T Med-Systems Cassette SystemC/T Med System, Ltd.1998—
−5K990761Tuttnauer Mini Container Cassette, Tuttnauer Standard Case CassetteTuttnauer U.S.A Co, Ltd.1999—
−4K012105Polyvac Surgical Instrument Delivery SystemSymmetry Medical, Inc.2002—
−3K023658Sterilization Cases and TraysCarr Metal Products, Inc.2003—
−2K052992Conmed Linvatec Instrument Sterilization TrayConmed Linvatec2006—
−1K070769VHP 136 TraySTERIS Corporation2007—
0 (this device)K140494V-Pro Sterilization Tray/ Sterilization MatSTERIS Corporation2014—
+1K160912Sterilization TraySTERIS Corporation2016—
+2K172755PRO-LITE Sterilization TraysSTERIS Corporation2018—
+3K183402PRO-LITE Sterilization TraySTERIS Corporation2019—
+4K222440Vis-U-All Low Temperature Sterilization Pouches/Tubing, PRO-LITE Sterilization…Steris2022—
+5K231501PRO-LITE Sterilization TraySTERIS Corporation2023—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199410
199710
200110
200210
200410
201110

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201610
201810
201920
202210
202320
FIG. 1 — Lineage of K140494, 1984–2023Source: 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 KCT? 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 KCT device

  1. #1 K214041 Aesculap AICON Containerscore 18.1 · 6 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? (2)

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
*K070769VHP 136 Tray
Summary page 2
…Class Il Product Code KCT 2. Predicate Device VHF® 136 Tray (renamed V-PRO Sterilization Tray) K070769 Sterilization Mat K103226 3. Descriition of Device The V-PRO Sterilization Tray is available in various size…
STERIS Corporation2007—
*K103226Sterilization Mats
Summary page 2
…Product Code KCT 2. Predicate Device VHF® 136 Tray (renamed V-PRO Sterilization Tray) K070769 Sterilization Mat K103226 3. Descriition of Device The V-PRO Sterilization Tray is available in various sizes, 10O"x 10" to 10" x 27" to…
STERIS Corporation2011—

Also cleared against K070769: 1 other device →

What descends from it? (7)

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

NumberDeviceApplicantDecidedDescendants
K160912Sterilization TraySTERIS Corporation20166

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 30 years and passes through 7 companies; a new generation was cleared every 3.1 years on median.
  • None of the 13 ancestors has a recall.
  • Of its descendants, K160912 (STERIS Corporation, 2016) has gone furthest, with 6 descendants of its own.
  • 1 other device also cites its predicate K070769.

How does its category compare?

All KCT devices

KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, this device’s year, is highlighted.

FDA decisions per year · KCT

11in 2025

2007: 32008: 62009: 62010: 122011: 62012: 102013: 82014: 112015: 152016: 122017: 102018: 152019: 182020: 142021: 182022: 112023: 102024: 82025: 112026 (partial year): 9
2007high 18 (2019) · low 3 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KCT

205in 2025

2007: 199 days median2008: 182 days median2009: 89 days median2010: 202 days median2011: 117 days median2012: 236 days median2013: 131 days median2014: 169 days median2015: 151 days median2016: 182 days median2017: 211 days median2018: 192 days median2019: 187 days median2020: 134 days median2021: 185 days median2022: 137 days median2023: 94 days median2024: 106 days median2025: 205 days median2026 (partial year): 122 days median
2007high 236 (2012) · low 89 (2009)2026

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

Recalls per year · KCT

17in 2022

2010: 12011: 22013: 12014: 12016: 32017: 12021: 12022: 17
2007high 17 (2022) · low 0 (2007)2026

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

Adverse event reports per year · KCT

50in 2025

2007: 22008: 82009: 52010: 32011: 32012: 22013: 62014: 52015: 62016: 162017: 32018: 222019: 152020: 662021: 262022: 82023: 302024: 182025: 50
2007high 66 (2020) · low 2 (2007)2025

MAUDE reports naming product code KCT, 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
2007319902
2008618208
200968905
20101220213
2011611723
20121023602
2013813116
20141116915
20151515106
201612182316
20171021113
201815192022
201918187015
202014134066
202118185126
202211137178
20231094030
20248106018
202511205050
202691220—

What is it indicated for?

The V-PRO Sterilization Tray is used to contain medical devices for sterilization in the Lumen, Non Lumen and Flexible Cycles of the V-PRO Low Temperature Sterilization Systems. The trays must be wrapped with a legally marketed sterilization wrap for use in the V-PRO Low Temperature Sterilization Systems prior to placing in the Sterilizer. The V-PRO Sterilization Tray is not intended to maintain sterility; it is intended to be used in conjunction with a…

Read the full statement (550 words)

The V-PRO Sterilization Tray is used to contain medical devices for sterilization in the Lumen, Non Lumen and Flexible Cycles of the V-PRO Low Temperature Sterilization Systems. The trays must be wrapped with a legally marketed sterilization wrap for use in the V-PRO Low Temperature Sterilization Systems prior to placing in the Sterilizer. The V-PRO Sterilization Tray is not intended to maintain sterility; it is intended to be used in conjunction with a validated, FDA-cleared sterilization wrap in order to maintain sterility of the enclosed medical instruments.

V-PRO 60 Lumen Cycle: Instruments with diffusion-restricted spaces such as the hinged portion of forceps and scissors; non-lumened devices including non-lumened rigid and semi-rigid endoscopes; medical devices, including single, dual and triple channeled rigid and semi-rigid endoscopes, with the following configurations: single or dual lumen devices, 0.77 mm ID and 410 mm in length; triple lumen devices, 1.2 mm ID and 275 mm in length, 1.8 mm ID and 310 mm in length, or 2.8 mm ID and 317 mm in length.

V-PRO 60 Non Lumen Cycle: Non-lumened devices including non-lumened rigid, semi-rigid and flexible endoscopes and non-lumened devices with stainless steel or titanium diffusion-restricted spaces such as the hinged portion of forceps and scissors.

V-PRO 60 Flexible Cycle: One flexible surgical endoscope or bronchoscope with a light cord (if not integral to endoscope) and mat without any additional load. The flexible endoscope may be a single or dual lumen device with lumens that are > 1 mm ID and < 990 mm in length.

V-PRO 1, 1 Plus & maX Lumen Cycle: Instruments with diffusion-restricted spaces such as the hinged portion of forceps and scissors; non-lumened devices including non-lumened rigid and semi-rigid endoscopes; medical devices, including single, dual and triple channeled rigid and semi-rigid endoscopes, with the following configurations: single or dual lumen devices, 0.77 mm ID and 527 mm in length; triple lumen devices, 1.2 mm ID and 275 mm in length, 1.8 mm ID and 310 mm in length, or 2.8 mm ID and 317 mm in length.

V-PRO 1 Plus & maX Non Lumen Cycle: Non-lumened devices including non-lumened rigid, semi-rigid and flexible endoscopes and non-lumened devices with stainless steel diffusion-restricted spaces such as the hinged portion of forceps and scissors.

V-PRO maX Flexible Cycle: Load 1: Single or dual lumen surgical flexible endoscopes (such as those used in ENT, Urology and Surgical Care) and bronchoscopes with a light cord (if not integral to endoscope) and mat with no additional load. The flexible endoscopes may contain either a single lumen that is > 1 mm ID and < 1050 mm in length, or two lumens with one lumen that is > 1 mm ID and < 990 mm in length and the other lumen that is > 1 mm ID and < 850 mm in length. Load 2: Non-lumened instruments including instruments with diffusion-restricted areas such as the hinged portion of forceps or scissors.

Optional instrument organizers are accessories to the trays and are intended to allow stabilization of various cylindrical medical devices during processing. The instrument organizers attach to the V-PRO Sterilization Tray base and stabilize cylindrical medical instruments.

Optional sterilization mats are accessories to the trays and are intended to be used in conjunction with the V-PRO Sterilization Trays to cushion and stabilize instruments within the trays.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K140494: V-Pro Sterilization Tray/ Sterilization Mat.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K140494

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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