510(k) Report

510(k) · Cleared

Cleared

Neodent Instruments Kits

K182865510(k) TraditionalCleared May 7, 2019208-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 May 7, 2019 as substantially equivalent to K171713 (Jjgc Industria E Comercio DE Materiais Dentarios S.A., 2018) after a 208-day review. Its family tree reaches back 9 generations to 1984. 13 later devices descend from it.

Decided
May 7, 2019
Review
208 days
Class
Class II
Product code
KCT
Recalls
None
Predicates
1

Its longest line of descent runs back 9 generations to K844002 (1984). 12 ancestors in all. 13 later devices descend from it, 4 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 backK142519 InterActive Complete Surgical TrayImplant Direct Sybron Manufacturing, LLC · 2015
  4. 2 generations backK160730 Instrument kitsAnthogyr · 2017
  5. 1 generation backK171713 Neodent Instrument KitsJjgc Industria E Comercio DE Materiais Dentarios S.A. · 2018
  6. This deviceK182865 Neodent Instruments KitsJjgc Industria E Comercio DE Materiais Dentarios S.A. · 2019
  7. Descendant · cites it directly · 5 of its ownK192670 Neodent Instrument Kit CasesJjgc Industria E Comercio DE Materiais Dentarios S.A. · 2019
  8. Descendant · cites it directly · 4 of its ownK201688 S.I.N. Instrument KitsS.I.N. - Sistema DE Implante Nacional S.A. · 2020
  9. Descendant · 2 generations on · 1 of its ownK212404 S.I.N. Instrument KitsS.I.N. - Sistema DE Implante Nacional S.A. · 2021
  10. Descendant · 2 generations on · 1 of its ownK203618 Neodent EasyGuide Kit CasesJjgc Industria E Comercio DE Materiais Dentarios S.A. · 2021
  11. Descendant · 3 generations on · 0 of its ownK241492 Guided Surgery Kit CasesJJGC Indústria e Comércio de Materiais Dentários S.A. · 2024
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 backK023658 Sterilization Cases and TraysCarr Metal Products, Inc. · 2003
  6. 4 generations backK052992 Conmed Linvatec Instrument Sterilization TrayConmed Linvatec · 2006
  7. 3 generations backK142519 InterActive Complete Surgical TrayImplant Direct Sybron Manufacturing, LLC · 2015
  8. 2 generations backK160730 Instrument kitsAnthogyr · 2017
  9. 1 generation backK171713 Neodent Instrument KitsJjgc Industria E Comercio DE Materiais Dentarios S.A. · 2018
  10. This deviceK182865 Neodent Instruments KitsJjgc Industria E Comercio DE Materiais Dentarios S.A. · 2019

Showing 5 of 13 descendants. See all descendants

Descendants cleared per year

2019: 12020: 22021: 32022: 32023: 22024: 2
2019high 3 (2021) · low 0 (2025)2026

Most influential descendants

Showing 5 of 13 · See all
  • K192670Neodent Instrument Kit CasesJjgc Industria E Comercio DE Materiais Dentarios S.A. · 2019 · cites it directly5descendants
  • K201688S.I.N. Instrument KitsS.I.N. - Sistema DE Implante Nacional S.A. · 2020 · cites it directly4descendants
  • K212404S.I.N. Instrument KitsS.I.N. - Sistema DE Implante Nacional S.A. · 2021 · 2 generations on1descendant
  • K203618Neodent EasyGuide Kit CasesJjgc Industria E Comercio DE Materiais Dentarios S.A. · 2021 · 2 generations on1descendant
  • K241492Guided Surgery Kit CasesJJGC Indústria e Comércio de Materiais Dentários S.A. · 2024 · 3 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—
−5K023658Sterilization Cases and TraysCarr Metal Products, Inc.2003—
−4K052992Conmed Linvatec Instrument Sterilization TrayConmed Linvatec2006—
−3K142519InterActive Complete Surgical TrayImplant Direct Sybron Manufacturing, LLC2015—
−2K160730Instrument kitsAnthogyr2017—
−1K171713Neodent Instrument KitsJjgc Industria E Comercio DE Materiais Dentarios S.A.2018—
0 (this device)K182865Neodent Instruments KitsJjgc Industria E Comercio DE Materiais Dentarios S.A.2019—
+1K192670Neodent Instrument Kit CasesJjgc Industria E Comercio DE Materiais Dentarios S.A.2019—
+1K201688S.I.N. Instrument KitsS.I.N. - Sistema DE Implante Nacional S.A.2020—
+2K212404S.I.N. Instrument KitsS.I.N. - Sistema DE Implante Nacional S.A.2021—
+2K203618Neodent EasyGuide Kit CasesJjgc Industria E Comercio DE Materiais Dentarios S.A.2021—
+3K241492Guided Surgery Kit CasesJJGC Indústria e Comércio de Materiais Dentários S.A.2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199410
199710
200110

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201910
202020
202130
202230
202320
202420
FIG. 1 — Lineage of K182865, 1984–2024Source: 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
*K171713Neodent Instrument Kits
Summary page 7
…ion Panel General Hospital Reviewing Branch Infection Control Devices Branch PREDICATE DEVICE INFORMATION Predicate Device K171713 – Neodent Instrument Kits, JJGC Indústria e Comércio de Materiais Dentários AS Reference Device…
Jjgc Industria E Comercio DE Materiais Dentarios S.A.2018—
†K142529Genesis Reusable Rigid Container SystemCarefusion 2200, Inc.20152
†K180915Sonicision Reusable Sterilization TrayCovidien2018—

Also cleared against K171713: 2 other devices →

What descends from it? (13)

See all 13

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

NumberDeviceApplicantDecidedDescendants
K192670Neodent Instrument Kit CasesJjgc Industria E Comercio DE Materiais Dentarios S.A.20195
K201688S.I.N. Instrument KitsS.I.N. - Sistema DE Implante Nacional S.A.20204
K230804Complement Kit CasesJJGC Indústria e Comércio de Materiais Dentários S.A.20230
K212068Biotech Dental KitsBiotech Dental, Sas20210

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 2.0 years on median.
  • None of the 12 ancestors has a recall.
  • Of its descendants, K192670 (Jjgc Industria E Comercio DE Materiais Dentarios S.A., 2019) has gone furthest, with 5 descendants of its own.
  • 2 other devices also cite its predicate K171713.

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?

Indications for Use for GM/WS Surgical Kit Case: 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…

Read the full statement (645 words)

Indications for Use for GM/WS Surgical Kit Case:

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 combined weight of the GM/WS Surgical Kit Case and the associated instruments is 674.5 g. The weight of the empty Kit Case is 507 grams.

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

Indications for Use for GM Prosthetic Kit Case:

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 combined weight of the GM Prosthetic Kit Case and the associated instruments is 250.5 g. The weight of the empty Kit Case is 210 grams.

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

Indications for Use for GM Try-In Kit Case:

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 require the use of FDA-cleared wrap to maintain the sterility of the enclosed devices.

The kits are to be enclosed in a sterilizable 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 combined weight of the GM Try-In Kit Case and the associated instruments is 212.6 g. The weight of the empty Kit Case is 195 grams.

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

Indications for Use for GM Guided Surgery Kit Case:

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, 40-minute dry time.

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

The combined weight of the GM Guided Surgery Surgical Kit Case and the associated instruments is 728.4 g. The weight of the empty Kit Case is 567 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. “K182865: Neodent Instruments Kits.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K182865

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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