510(k) Report

510(k) · Cleared

Cleared

Straumann Modular Cassette

K191522510(k) TraditionalCleared Dec 3, 2019176-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

Institut Straumann AG · KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

Cleared on Dec 3, 2019 as substantially equivalent to K180791 (Institut Straumann AG, 2018) after a 176-day review. Its family tree reaches back 9 generations to 1984. 2 later devices descend from it.

Decided
Dec 3, 2019
Review
176 days
Class
Class II
Product code
KCT
Recalls
None
Predicates
1

Its longest line of descent runs back 9 generations to K844002 (1984). 15 ancestors in all. 2 later devices descend from it, 1 citing it directly.

  1. Root · 9 generations backK844002 HU-Friedy Ims Cassette SystemHu-Friedy Mfg. Co., Inc. · 1984
  2. 5 generations between
  3. 3 generations backK152241 Medtronic Transportation/Sterilization CassettesMedtronic Sofamor Danek USA, Inc. · 2016
  4. 2 generations backK163600 Kit Boxes and Kit PlatesNobel Biocare AB · 2018
  5. 1 generation backK180791 Straumann BLX Surgical CassetteInstitut Straumann AG · 2018
  6. This deviceK191522 Straumann Modular CassetteInstitut Straumann AG · 2019
  7. Descendant · cites it directly · 1 of its ownK203753 Straumann Surgical CassettesStraumann USA, LLC · 2021
  8. Descendant · 2 generations on · 0 of its ownK233264 Anthogyr INTEGRAL Guided Surgery CassettesAnthogyr · 2023
Show all 9 generations
  1. Root · 9 generations backK844002 HU-Friedy Ims Cassette SystemHu-Friedy Mfg. Co., Inc. · 1984
  2. 8 generations backK980065 C/T Med-Systems Cassette SystemC/T Med System, Ltd. · 1998
  3. 7 generations backK990761 Tuttnauer Mini Container Cassette, Tuttnauer Standard Case CassetteTuttnauer U.S.A Co, Ltd. · 1999
  4. 6 generations backK012105 Polyvac Surgical Instrument Delivery SystemSymmetry Medical, Inc. · 2002
  5. 5 generations backK040223 Polyvac Instrument Delivery SystemSymmetry Medical USA, Inc. · 2004
  6. 4 generations backK120947 THS Instrument TrayHologic, Inc. · 2012
  7. 3 generations backK152241 Medtronic Transportation/Sterilization CassettesMedtronic Sofamor Danek USA, Inc. · 2016
  8. 2 generations backK163600 Kit Boxes and Kit PlatesNobel Biocare AB · 2018
  9. 1 generation backK180791 Straumann BLX Surgical CassetteInstitut Straumann AG · 2018
  10. This deviceK191522 Straumann Modular CassetteInstitut Straumann AG · 2019

Most influential descendants

Showing 2 of 2 · See all
  • K203753Straumann Surgical CassettesStraumann USA, LLC · 2021 · cites it directly1descendant
  • K233264Anthogyr INTEGRAL Guided Surgery CassettesAnthogyr · 2023 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−9K844002HU-Friedy Ims Cassette SystemHu-Friedy Mfg. Co., Inc.1984—
−8K980065C/T Med-Systems Cassette SystemC/T Med System, Ltd.1998—
−7K990761Tuttnauer Mini Container Cassette, Tuttnauer Standard Case CassetteTuttnauer U.S.A Co, Ltd.1999—
−6K012105Polyvac Surgical Instrument Delivery SystemSymmetry Medical, Inc.2002—
−5K040223Polyvac Instrument Delivery SystemSymmetry Medical USA, Inc.2004—
−4K120947THS Instrument TrayHologic, Inc.2012—
−3K152241Medtronic Transportation/Sterilization CassettesMedtronic Sofamor Danek USA, Inc.2016—
−2K163600Kit Boxes and Kit PlatesNobel Biocare AB2018—
−1K180791Straumann BLX Surgical CassetteInstitut Straumann AG2018—
0 (this device)K191522Straumann Modular CassetteInstitut Straumann AG2019—
+1K203753Straumann Surgical CassettesStraumann USA, LLC2021—
+2K233264Anthogyr INTEGRAL Guided Surgery CassettesAnthogyr2023—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199410
199710
200110
200210
200410
201310

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202110
202310
FIG. 1 — Lineage of K191522, 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? (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
*K180791Straumann BLX Surgical Cassette
Summary page 5
…l 510(k) Submission Straumann Modular Cassette K191522 Predicate Device(s) Primary Predicate: • K180791 - Straumann BLX Surgical Cassette Device Description Straumann Modular Cassette consists of three modules: A, B and C module. Th…
Institut Straumann AG2018—

Also cleared against K180791: 4 other devices →

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K203753Straumann Surgical CassettesStraumann USA, LLC20211

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 35 years and passes through 9 companies; a new generation was cleared every 2.2 years on median.
  • None of the 15 ancestors has a recall.
  • Of its descendants, K203753 (Straumann USA, LLC, 2021) has gone furthest, with 1 descendant of its own.
  • 4 other devices also cite its predicate K180791.

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. 2019, 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?

Straumann® Modular Cassette is used in healthcare facilities to organize, enclose, sterilize, transport and store Straumann instruments between surgical uses. Straumann® Modular Cassette is not intended to maintain sterility on its own, but is intended to be used in conjunction with a legally marketed, validated sterilization double pouch to maintain the sterility of the enclosed devices. The Straumann® Modular Cassette has been validated for the…

Read the full statement (177 words)

Straumann® Modular Cassette is used in healthcare facilities to organize, enclose, sterilize, transport and store Straumann instruments between surgical uses.

Straumann® Modular Cassette is not intended to maintain sterility on its own, but is intended to be used in conjunction with a legally marketed, validated sterilization double pouch to maintain the sterility of the enclosed devices.

The Straumann® Modular Cassette has been validated for the following maximum loads:

• Module A 400g

• BCC Maximum permissible stack BCC 611g

The A module is intended to be sterilized individually, without stacking with other modules.

The B and C module are intended to be sterilized individually, or by stacking the B module on top of C module bases. The maximum permissible stack for sterilization is one B module on top of two C module bases.

The B module lid and C module lid could be used to enclose an ultrasonic mat (Art. No. 041.774) for ultrasonic bath cleaning used instruments.

Only use the following sterilization parameters:

• Pre-vacuum: 132°C (270 °F) for 4 minutes with 30 minutes drying time

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K191522: Straumann Modular Cassette.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K191522

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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