510(k) Report

510(k) · Cleared

Cleared

Neodent Instrument Kits

K171713510(k) TraditionalCleared Apr 5, 2018300-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

Jjgc Industria E Comercio DE Materiais Dentarios S.A. · KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

Cleared on Apr 5, 2018 as substantially equivalent to K160730 (Anthogyr, 2017) after a 300-day review. Its family tree reaches back 8 generations to 1984. 18 later devices descend from it.

Decided
Apr 5, 2018
Review
300 days
Class
Class II
Product code
KCT
Recalls
None
Predicates
1

Its longest line of descent runs back 8 generations to K844002 (1984). 11 ancestors in all. 18 later devices descend from it, 3 citing it directly.

  1. Root · 8 generations backK844002 HU-Friedy Ims Cassette SystemHu-Friedy Mfg. Co., Inc. · 1984
  2. 7 generations backK980065 C/T Med-Systems Cassette SystemC/T Med System, Ltd. · 1998
  3. 6 generations backK990761 Tuttnauer Mini Container Cassette, Tuttnauer Standard Case CassetteTuttnauer U.S.A Co, Ltd. · 1999
  4. 5 generations backK012105 Polyvac Surgical Instrument Delivery SystemSymmetry Medical, Inc. · 2002
  5. 4 generations backK023658 Sterilization Cases and TraysCarr Metal Products, Inc. · 2003
  6. 3 generations backK052992 Conmed Linvatec Instrument Sterilization TrayConmed Linvatec · 2006
  7. 2 generations backK142519 InterActive Complete Surgical TrayImplant Direct Sybron Manufacturing, LLC · 2015
  8. 1 generation backK160730 Instrument kitsAnthogyr · 2017
  9. This deviceK171713 Neodent Instrument KitsJjgc Industria E Comercio DE Materiais Dentarios S.A. · 2018
  10. Descendant · cites it directly · 13 of its ownK182865 Neodent Instruments KitsJjgc Industria E Comercio DE Materiais Dentarios S.A. · 2019
  11. Descendant · 2 generations on · 5 of its ownK192670 Neodent Instrument Kit CasesJjgc Industria E Comercio DE Materiais Dentarios S.A. · 2019
  12. Descendant · 2 generations on · 4 of its ownK201688 S.I.N. Instrument KitsS.I.N. - Sistema DE Implante Nacional S.A. · 2020
  13. Descendant · cites it directly · 2 of its ownK201878 ST-Z5Z-Systems AG · 2021
  14. Descendant · 3 generations on · 1 of its ownK212404 S.I.N. Instrument KitsS.I.N. - Sistema DE Implante Nacional S.A. · 2021

Showing 5 of 18 descendants. See all descendants

Descendants cleared per year

2019: 32020: 22021: 42022: 32023: 22024: 22025: 2
2019high 4 (2021) · low 0 (2026)2026

Most influential descendants

Showing 5 of 18 · See all
  • K182865Neodent Instruments KitsJjgc Industria E Comercio DE Materiais Dentarios S.A. · 2019 · cites it directly13descendants
  • K192670Neodent Instrument Kit CasesJjgc Industria E Comercio DE Materiais Dentarios S.A. · 2019 · 2 generations on5descendants
  • K201688S.I.N. Instrument KitsS.I.N. - Sistema DE Implante Nacional S.A. · 2020 · 2 generations on4descendants
  • K201878ST-Z5Z-Systems AG · 2021 · cites it directly2descendants
  • K212404S.I.N. Instrument KitsS.I.N. - Sistema DE Implante Nacional S.A. · 2021 · 3 generations on1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K844002HU-Friedy Ims Cassette SystemHu-Friedy Mfg. Co., Inc.1984—
−7K980065C/T Med-Systems Cassette SystemC/T Med System, Ltd.1998—
−6K990761Tuttnauer Mini Container Cassette, Tuttnauer Standard Case CassetteTuttnauer U.S.A Co, Ltd.1999—
−5K012105Polyvac Surgical Instrument Delivery SystemSymmetry Medical, Inc.2002—
−4K023658Sterilization Cases and TraysCarr Metal Products, Inc.2003—
−3K052992Conmed Linvatec Instrument Sterilization TrayConmed Linvatec2006—
−2K142519InterActive Complete Surgical TrayImplant Direct Sybron Manufacturing, LLC2015—
−1K160730Instrument kitsAnthogyr2017—
0 (this device)K171713Neodent Instrument KitsJjgc Industria E Comercio DE Materiais Dentarios S.A.2018—
+1K182865Neodent Instruments KitsJjgc Industria E Comercio DE Materiais Dentarios S.A.2019—
+2K192670Neodent Instrument Kit CasesJjgc Industria E Comercio DE Materiais Dentarios S.A.2019—
+2K201688S.I.N. Instrument KitsS.I.N. - Sistema DE Implante Nacional S.A.2020—
+1K201878ST-Z5Z-Systems AG2021—
+3K212404S.I.N. Instrument KitsS.I.N. - Sistema DE Implante Nacional S.A.2021—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199410
199710
200110

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201930
202020
202140
202230
202320
202420
202520
FIG. 1 — Lineage of K171713, 1984–2025Source: 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
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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
*K160730Instrument kits
Summary page 4
…ification Panel General Hospital Reviewing Branch General Hospital PREDICATE DEVICE INFORMATION The primary predicate device is K160730, Instrument Kits, Anthogyr. Page 1 of 4 510(k) Summary…
Anthogyr2017—

Also cleared against K160730: 1 other device →

What descends from it? (18)

See all 18

3 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K182865Neodent Instruments KitsJjgc Industria E Comercio DE Materiais Dentarios S.A.201913
K201878ST-Z5Z-Systems AG20212
K190665Neodent Instrument Kit CasesJjgc Industria E Comercio DE Materiais Dentarios S.A.20190

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 34 years and passes through 9 companies; a new generation was cleared every 3.1 years on median.
  • None of the 11 ancestors has a recall.
  • Of its descendants, K182865 (Jjgc Industria E Comercio DE Materiais Dentarios S.A., 2019) has gone furthest, with 13 descendants of its own.
  • 1 other device also cites its predicate K160730.

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. 2018, 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?

Neodent Instrument Kits are intended to be used to enclose other medical devices that are to be sterilized by a health care provider. Neodent Instrument Kits are intended to allow sterilization of the enclosed medical devices. Neodent Instrument Kits require the use of FDA cleared wrap to maintain the sterility of the enclosed devices. The kits are to be enclosed in a sterilization wrap that is FDA-cleared for the indicated cycles, and moist heat (steam)…

Read the full statement (154 words)

Neodent Instrument Kits are intended to be used to enclose other medical devices that are to be sterilized by a health care provider. Neodent Instrument Kits are intended to allow sterilization of the enclosed medical devices. Neodent Instrument Kits require the use of FDA cleared wrap to maintain the sterility of the enclosed devices.

The kits are to be enclosed in a sterilization wrap that is FDA-cleared for the indicated cycles, and moist heat (steam) sterilized using one of the following cycles:

Fractionated vacuum (pre-vacuum) — Exposure at 132 °C for 4 minutes, 20 minute dry time

Gravity displacement — Exposure at 132 °C for 15 minutes, 20 minute dry time

Neodent Instrument Kits are intended for sterilization of non-porous loads.

The GM/WS Surgical Kit Case maximum load weight is 125 grams.

The GM Surgical Kit Case maximum load weight is 113 grams.

Neodent Instrument Kits are recommended not to be stacked during sterilization.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K171713: Neodent Instrument Kits.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K171713

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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