510(k) Report

510(k) · Cleared

Cleared

S.I.N. Instrument Kits

K201688510(k) TraditionalCleared Oct 21, 2020121-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

S.I.N. - Sistema DE Implante Nacional S.A. · KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

Cleared on Oct 21, 2020 as substantially equivalent to K182865 (Jjgc Industria E Comercio DE Materiais Dentarios S.A., 2019) after a 121-day review. Its family tree reaches back 10 generations to 1984. 4 later devices descend from it.

Decided
Oct 21, 2020
Review
121 days
Class
Class II
Product code
KCT
Recalls
None
Predicates
1

Its longest line of descent runs back 10 generations to K844002 (1984). 13 ancestors in all. 4 later devices descend from it, 4 citing it directly.

  1. Root · 10 generations backK844002 HU-Friedy Ims Cassette SystemHu-Friedy Mfg. Co., Inc. · 1984
  2. 6 generations between
  3. 3 generations backK160730 Instrument kitsAnthogyr · 2017
  4. 2 generations backK171713 Neodent Instrument KitsJjgc Industria E Comercio DE Materiais Dentarios S.A. · 2018
  5. 1 generation backK182865 Neodent Instruments KitsJjgc Industria E Comercio DE Materiais Dentarios S.A. · 2019
  6. This deviceK201688 S.I.N. Instrument KitsS.I.N. - Sistema DE Implante Nacional S.A. · 2020
  7. Descendant · cites it directly · 1 of its ownK212404 S.I.N. Instrument KitsS.I.N. - Sistema DE Implante Nacional S.A. · 2021
  8. Descendant · cites it directly · 0 of its ownK241378 S.I.N. Instrument KitsS.I.N. - Sistema DE Implante Nacional S.A. · 2024
  9. Descendant · cites it directly · 0 of its ownK222514 S.I.N. Instrument KitsS.I.N. – Sistema DE Implante Nacional S.A. · 2022
  10. Descendant · cites it directly · 0 of its ownK222005 S.I.N. Instrument KitsS.I.N. - Sistema DE Implante Nacional S.A. · 2022
Show all 10 generations
  1. Root · 10 generations backK844002 HU-Friedy Ims Cassette SystemHu-Friedy Mfg. Co., Inc. · 1984
  2. 9 generations backK980065 C/T Med-Systems Cassette SystemC/T Med System, Ltd. · 1998
  3. 8 generations backK990761 Tuttnauer Mini Container Cassette, Tuttnauer Standard Case CassetteTuttnauer U.S.A Co, Ltd. · 1999
  4. 7 generations backK012105 Polyvac Surgical Instrument Delivery SystemSymmetry Medical, Inc. · 2002
  5. 6 generations backK023658 Sterilization Cases and TraysCarr Metal Products, Inc. · 2003
  6. 5 generations backK052992 Conmed Linvatec Instrument Sterilization TrayConmed Linvatec · 2006
  7. 4 generations backK142519 InterActive Complete Surgical TrayImplant Direct Sybron Manufacturing, LLC · 2015
  8. 3 generations backK160730 Instrument kitsAnthogyr · 2017
  9. 2 generations backK171713 Neodent Instrument KitsJjgc Industria E Comercio DE Materiais Dentarios S.A. · 2018
  10. 1 generation backK182865 Neodent Instruments KitsJjgc Industria E Comercio DE Materiais Dentarios S.A. · 2019
  11. This deviceK201688 S.I.N. Instrument KitsS.I.N. - Sistema DE Implante Nacional S.A. · 2020

Most influential descendants

Showing 4 of 4 · See all
  • K212404S.I.N. Instrument KitsS.I.N. - Sistema DE Implante Nacional S.A. · 2021 · cites it directly1descendant
  • K241378S.I.N. Instrument KitsS.I.N. - Sistema DE Implante Nacional S.A. · 2024 · cites it directly0descendants
  • K222514S.I.N. Instrument KitsS.I.N. – Sistema DE Implante Nacional S.A. · 2022 · cites it directly0descendants
  • K222005S.I.N. Instrument KitsS.I.N. - Sistema DE Implante Nacional S.A. · 2022 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−10K844002HU-Friedy Ims Cassette SystemHu-Friedy Mfg. Co., Inc.1984—
−9K980065C/T Med-Systems Cassette SystemC/T Med System, Ltd.1998—
−8K990761Tuttnauer Mini Container Cassette, Tuttnauer Standard Case CassetteTuttnauer U.S.A Co, Ltd.1999—
−7K012105Polyvac Surgical Instrument Delivery SystemSymmetry Medical, Inc.2002—
−6K023658Sterilization Cases and TraysCarr Metal Products, Inc.2003—
−5K052992Conmed Linvatec Instrument Sterilization TrayConmed Linvatec2006—
−4K142519InterActive Complete Surgical TrayImplant Direct Sybron Manufacturing, LLC2015—
−3K160730Instrument kitsAnthogyr2017—
−2K171713Neodent Instrument KitsJjgc Industria E Comercio DE Materiais Dentarios S.A.2018—
−1K182865Neodent Instruments KitsJjgc Industria E Comercio DE Materiais Dentarios S.A.2019—
0 (this device)K201688S.I.N. Instrument KitsS.I.N. - Sistema DE Implante Nacional S.A.2020—
+1K212404S.I.N. Instrument KitsS.I.N. - Sistema DE Implante Nacional S.A.2021—
+1K241378S.I.N. Instrument KitsS.I.N. - Sistema DE Implante Nacional S.A.2024—
+1K222514S.I.N. Instrument KitsS.I.N. – Sistema DE Implante Nacional S.A.2022—
+1K222005S.I.N. Instrument KitsS.I.N. - Sistema DE Implante Nacional S.A.2022—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199410
199710
200110

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202110
202220
202410
FIG. 1 — Lineage of K201688, 1984–2024Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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
*K182865Neodent Instruments Kits
Summary page 17
…wing Division Division of Infection Control and Plastic Surgery Devices (DHT4B) PREDICATE DEVICE INFORMATION The primary predicate device is: K182865, Neodent Instrument Kits, JJGC Indústria e Comércio de Materiais Dentários S.A. Page 2 of 10 SUBJECT DEVICE…
Jjgc Industria E Comercio DE Materiais Dentarios S.A.2019—

Also cleared against K182865: 3 other devices →

What descends from it? (4)

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

NumberDeviceApplicantDecidedDescendants
K212404S.I.N. Instrument KitsS.I.N. - Sistema DE Implante Nacional S.A.20211
K241378S.I.N. Instrument KitsS.I.N. - Sistema DE Implante Nacional S.A.20240
K222514S.I.N. Instrument KitsS.I.N. – Sistema DE Implante Nacional S.A.20220
K222005S.I.N. Instrument KitsS.I.N. - Sistema DE Implante Nacional S.A.20220

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 36 years and passes through 10 companies; a new generation was cleared every 2.0 years on median.
  • None of the 13 ancestors has a recall.
  • Of its descendants, K212404 (S.I.N. - Sistema DE Implante Nacional S.A., 2021) has gone furthest, with 1 descendant of its own.
  • 3 other devices also cite its predicate K182865.

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. 2020, 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 Safe Drill Unitite Kit S.I.N. Instrument Kits are intended to be used to enclose other medical devices that are to be sterilized by a health care provider. S.I.N. Instrument Kits are intended to allow sterilization of the enclosed medical devices. S.I.N. Instrument Kits require the use of a wrap that is FDA cleared to maintain the sterility of the enclosed devices. The kits are to be enclosed in a sterilization wrap that is FDA…

Read the full statement (2,166 words)

Indications for Use for Safe Drill Unitite Kit

S.I.N. Instrument Kits are intended to be used to enclose other medical devices that are to be sterilized by a health care provider. S.I.N. Instrument Kits are intended to allow sterilization of the enclosed medical devices. S.I.N. Instrument Kits require the use of a wrap that is FDA cleared 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 the following cycle:

Gravity displacement – Exposure at 121 °C for 30 minutes and 30 minutes dry time.

S.I.N. Instrument Kits are intended for sterilization of non-porous loads.

S.I.N. Instrument Kits are recommended not to be stacked during sterilization.

The combined weight of the Safe Drill Unitite Kit and the associated instruments is 304 grams.

The weight of the empty Safe Drill Unitite Kit is 150 grams.

Indications for Use for Safe Drill SW Kit

S.I.N. Instrument Kits are intended to be used to enclose other medical devices that are to be sterilized by a health care provider. S.I.N. Instrument Kits are intended to allow sterilization of the enclosed medical devices. S.I.N. Instrument Kits require the use of a wrap that is FDA cleared 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 the following cycle:

Gravity displacement – Exposure at 121 °C for 30 minutes and 30 minutes dry time.

S.I.N. Instrument Kits are intended for sterilization of non-porous loads.

S.I.N. Instrument Kits are recommended not to be stacked during sterilization.

The combined weight of the Safe Drill SW Kit and the associated instruments is 278 grams.

The weight of the empty Safe Drill SW Kit is 138 grams.

Indications for Use for Prosthetic Kit

S.I.N. Instrument Kits are intended to be used to enclose other medical devices that are to be sterilized by a health care provider. S.I.N. Instrument Kits are intended to allow sterilization of the enclosed medical devices. S.I.N. Instrument Kits require the use of a wrap that is FDA cleared 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 the following cycle:

Gravity displacement – Exposure at 121 °C for 30 minutes and 30 minutes dry time.

S.I.N. Instrument Kits are intended for sterilization of non-porous loads.

S.I.N. Instrument Kits are recommended not to be stacked during sterilization.

The combined weight of the Prosthetic Kit and the associated instruments is 332 grams.

The weight of the empty Prosthetic Kit is 160 grams.

Indications for Use for Rotatory Expanding Kit

S.I.N. Instrument Kits are intended to be used to enclose other medical devices that are to be sterilized by a health care provider. S.I.N. Instrument Kits are intended to allow sterilization of the enclosed medical devices. S.I.N. Instrument Kits require the use of a wrap that is FDA cleared 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 the following cycle:

Gravity displacement – Exposure at 121 °C for 30 minutes and 30 minutes dry time.

S.I.N. Instrument Kits are intended for sterilization of non-porous loads.

S.I.N. Instrument Kits are recommended not to be stacked during sterilization.

The combined weight of the Rotatory Expanding Kit and the associated instruments is 276 grams.

The weight of the empty Rotatory Expanding Kit is 133 grams.

Indications for Use for Bone Expander Kit

S.I.N. Instrument Kits are intended to be used to enclose other medical devices that are to be sterilized by a health care provider. S.I.N. Instrument Kits are intended to allow sterilization of the enclosed medical devices. S.I.N. Instrument Kits require the use of a wrap that is FDA cleared 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 the following cycle:

Gravity displacement – Exposure at 121 °C for 30 minutes and 30 minutes dry time.

S.I.N. Instrument Kits are intended for sterilization of non-porous loads.

S.I.N. Instrument Kits are recommended not to be stacked during sterilization.

The combined weight of the Bone Expander Kit and the associated instruments is 974 grams.

The weight of the empty Bone Expander Kit is 367 grams.

Indications for Use for Sinus Lift Kit

S.I.N. Instrument Kits are intended to be used to enclose other medical devices that are to be sterilized by a health care provider. S.I.N. Instrument Kits are intended to allow sterilization of the enclosed medical devices. S.I.N. Instrument Kits require the use of a wrap that is FDA cleared 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 the following cycle:

Gravity displacement – Exposure at 121 °C for 30 minutes and 30 minutes dry time.

S.I.N. Instrument Kits are intended for sterilization of non-porous loads.

S.I.N. Instrument Kits are recommended not to be stacked during sterilization.

The combined weight of the Sinus Lift Kit and the associated instruments is 808 grams.

The weight of the empty Sinus Lift Kit is 370 grams.

Indications for Use for Osteotome Kit

S.I.N. Instrument Kits are intended to be used to enclose other medical devices that are to be sterilized by a health care provider. S.I.N. Instrument Kits are intended to allow sterilization of the enclosed medical devices. S.I.N. Instrument Kits require the use of a wrap that is FDA cleared 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 the following cycle:

Gravity displacement – Exposure at 121 °C for 30 minutes and 30 minutes dry time.

S.I.N. Instrument Kits are intended for sterilization of non-porous loads.

S.I.N. Instrument Kits are recommended not to be stacked during sterilization.

The combined weight of the Osteotome Kit and the associated instruments is 957 grams.

The weight of the empty Osteotome Kit is 350 grams.

Indications for Use for Unitite Surgical Kit

S.I.N. Instrument Kits are intended to be used to enclose other medical devices that are to be sterilized by a health care provider. S.I.N. Instrument Kits are intended to allow sterilization of the enclosed medical devices. S.I.N. Instrument Kits require the use of a wrap that is FDA cleared 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 the following cycle:

Gravity displacement – Exposure at 121 °C for 30 minutes and 30 minutes dry time.

S.I.N. Instrument Kits are intended for sterilization of non-porous loads.

S.I.N. Instrument Kits are recommended not to be stacked during sterilization.

The combined weight of the Unitite Surgical Kit and the associated instruments is 1126 grams.

The weight of the empty Unitite Surgical Kit is 515 grams.

Indications for Use for Strong SW Surgical Kit

S.I.N. Instrument Kits are intended to be used to enclose other medical devices that are to be sterilized by a health care provider. S.I.N. Instrument Kits are intended to allow sterilization of the enclosed medical devices. S.I.N. Instrument Kits require the use of a wrap that is FDA cleared 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 the following cycle:

Gravity displacement – Exposure at 121 °C for 30 minutes and 30 minutes dry time.

S.I.N. Instrument Kits are intended for sterilization of non-porous loads.

S.I.N. Instrument Kits are recommended not to be stacked during sterilization.

The combined weight of the Strong SW Surgical Kit and the associated instruments is 698 grams.

The weight of the empty Strong SW Surgical Kit is 130 grams.

Indications for Use for Tryon Surgical Kit KCHE 03

S.I.N. Instrument Kits are intended to be used to enclose other medical devices that are to be sterilized by a health care provider. S.I.N. Instrument Kits are intended to allow sterilization of the enclosed medical devices. S.I.N. Instrument Kits require the use of a wrap that is FDA cleared 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 the following cycle:

Gravity displacement – Exposure at 121 °C for 30 minutes and 30 minutes dry time.

S.I.N. Instrument Kits are intended for sterilization of non-porous loads.

S.I.N. Instrument Kits are recommended not to be stacked during sterilization.

The combined weight of the Tryon Surgical Kit KCHE 03 and the associated instruments is 1127 grams.

The weight of the empty Tryon Surgical Kit KCHE 03 is 520 grams.

Indications for Use for Tryon Surgical Kit KCHE 04

S.I.N. Instrument Kits are intended to be used to enclose other medical devices that are to be sterilized by a health care provider. S.I.N. Instrument Kits are intended to allow sterilization of the enclosed medical devices. S.I.N. Instrument Kits require the use of a wrap that is FDA cleared 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 the following cycle:

Gravity displacement – Exposure at 121 °C for 30 minutes and 30 minutes dry time.

S.I.N. Instrument Kits are intended for sterilization of non-porous loads.

S.I.N. Instrument Kits are recommended not to be stacked during sterilization.

The combined weight of the Tryon Surgical Kit KCHE 04 and the associated instruments is 1138 grams.

The weight of the empty Tryon Surgical Kit KCHE 04 is 523 grams.

Indications for Use for Unitite Surgical Guided Kit

S.I.N. Instrument Kits are intended to be used to enclose other medical devices that are to be sterilized by a health care provider. S.I.N. Instrument Kits are intended to allow sterilization of the enclosed medical devices. S.I.N. Instrument Kits require the use of a wrap that is FDA cleared 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 the following cycle:

Gravity displacement – Exposure at 121 °C for 30 minutes and 30 minutes dry time.

S.I.N. Instrument Kits are intended for sterilization of non-porous loads.

S.I.N. Instrument Kits are recommended not to be stacked during sterilization.

The combined weight of the Unitite Surgical Guided Kit and the associated instruments is 1434 grams.

The weight of the empty Unitite Surgical Guided Kit is 650 grams.

Indications for Use for Strong SW Surgical Guided Kit

S.I.N. Instrument Kits are intended to be used to enclose other medical devices that are to be sterilized by a health care provider. S.I.N. Instrument Kits are intended to allow sterilization of the enclosed medical devices. S.I.N. Instrument Kits require the use of a wrap that is FDA cleared 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 the following cycle:

Gravity displacement – Exposure at 121 °C for 30 minutes and 30 minutes dry time.

S.I.N. Instrument Kits are intended for sterilization of non-porous loads.

S.I.N. Instrument Kits are recommended not to be stacked during sterilization.

The combined weight of the Strong SW Surgical Guided Kit and the associated instruments is 1399 grams.

The weight of the empty Strong SW Surgical Guided Kit is 647 grams.

Indications for Use for Zygomatic Surgical Kit

S.I.N. Instrument Kits are intended to be used to enclose other medical devices that are to be sterilized by a health care provider. S.I.N. Instrument Kits are intended to allow sterilization of the enclosed medical devices. S.I.N. Instrument Kits require the use of a wrap that is FDA cleared 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 the following cycle:

Gravity displacement – Exposure at 121 °C for 30 minutes and 30 minutes dry time.

S.I.N. Instrument Kits are intended for sterilization of non-porous loads.

S.I.N. Instrument Kits are recommended not to be stacked during sterilization.

The combined weight of the Zygomatic Surgical Kit and the associated instruments is 1150 grams.

The weight of the empty Zygomatic Surgical Kit is 464 grams.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K201688: S.I.N. 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/K201688

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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