510(k) Report

510(k) · Cleared

Cleared

IBS Implant System II

K200753510(k) SpecialCleared Jun 9, 202078-day reviewClass II21 CFR 872.3630

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

Innobiosurg Co., Ltd. · NHA Abutment, Implant, Dental, Endosseous

Cleared on Jun 9, 2020 as substantially equivalent to K162099 (Innobiosurg Co., Ltd., 2017) after a 78-day review. Its family tree reaches back 15 generations to 1990. 1 later device descends from it.

Decided
Jun 9, 2020
Review
78 days
Class
Class II
Product code
NHA
Recalls
None
Predicates
1

Its longest line of descent runs back 15 generations to K894595 (1990). 102 ancestors in all, the oldest K894844 (1990). 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2015: 1 other ancestor2013: 1 other ancestor2011: 2 other ancestors2012: 2 other ancestors2010: 4 other ancestors2009: 1 other ancestor2008: 7 other ancestors2007: 6 other ancestors2006: 6 other ancestors2005: 3 other ancestors2004: 5 other ancestors2003: 4 other ancestors2002: 9 other ancestors1996: 6 other ancestors2001: 7 other ancestors2000: 2 other ancestors1999: 6 other ancestors1997: 4 other ancestors1994: 3 other ancestors1998: 2 other ancestors1995: 1 other ancestor1993: 2 other ancestors1992: 1 other ancestor1990: 2 other ancestors2022: 1 descendant clearedReference device: K140806 · Ibs Implant System · Innobiosurg Co., Ltd. · 2015K894595 · Bonefit R Screw Implants · Institut Straumann AG · 1990K984104 · Iti Dental Implant System · Straumann USA · 1999 · recalledK993595 · Nobel Biocare's Modified Surface Implant (Intended for Immediate Loading Upon Placement) · Nobel Biocare Uas, Inc. · 2000K011879 · 3A Dental Implant System · Osseco Biosource, Ltd. · 2002K051576 · Avana Dental Implant System · Osstem Co., Ltd. · 2005K062051 · SS System · Osstem Implant Co., Ltd. · 2006K063861 · GS System · Osstem Implant Co., Ltd. · 2007×2: 2 generations cleared close together, K080744 (2008), K082213 (2008) K093352 · HG Iii Fixture System · Hiossen, Inc. · 2009K101096 · HT Iii SA Fixture System · Hiossen, Inc. · 2010K121585 · TS Implant System · Osstem Implant Co., Ltd. · 2013K140507 · Hiossen Prosthetic System · Osstem Implant Co., Ltd. · 2014K153350 · IBS Implant System · Innobiosurg Co., Ltd. · 2016K162099 · IBS Implant System II · Innobiosurg Co., Ltd. · 20171990200020102020
  1. Root · 15 generations backK894595 Bonefit R Screw ImplantsInstitut Straumann AG · 1990
  2. 11 generations between
  3. 3 generations backK140507 Hiossen Prosthetic SystemOsstem Implant Co., Ltd. · 2014
  4. 2 generations backK153350 IBS Implant SystemInnobiosurg Co., Ltd. · 2016
  5. 1 generation backK162099 IBS Implant System IIInnobiosurg Co., Ltd. · 2017
  6. This deviceK200753 IBS Implant System IIInnobiosurg Co., Ltd. · 2020
  7. Descendant · cites it directly · 0 of its ownK220517 IBS SystemInnobiosurg Co., Ltd. · 2022
Show all 15 generations
  1. Root · 15 generations backK894595 Bonefit R Screw ImplantsInstitut Straumann AG · 1990
  2. 14 generations backK984104 Iti Dental Implant SystemStraumann USA · 1999 · Recalled
  3. 13 generations backK993595 Nobel Biocare's Modified Surface Implant (Intended for Immediate…Nobel Biocare Uas, Inc. · 2000
  4. 12 generations backK011879 3A Dental Implant SystemOsseco Biosource, Ltd. · 2002
  5. 11 generations backK051576 Avana Dental Implant SystemOsstem Co., Ltd. · 2005
  6. 10 generations backK062051 SS SystemOsstem Implant Co., Ltd. · 2006
  7. 9 generations backK063861 GS SystemOsstem Implant Co., Ltd. · 2007
  8. 8 generations backK080744 HG II Fixture SystemOsstem Implant Co., Ltd. · 2008
  9. 7 generations backK082213 GS Iii Fixture SystemOsstem Implant Co., Ltd. · 2008
  10. 6 generations backK093352 HG Iii Fixture SystemHiossen, Inc. · 2009
  11. 5 generations backK101096 HT Iii SA Fixture SystemHiossen, Inc. · 2010
  12. 4 generations backK121585 TS Implant SystemOsstem Implant Co., Ltd. · 2013
  13. 3 generations backK140507 Hiossen Prosthetic SystemOsstem Implant Co., Ltd. · 2014
  14. 2 generations backK153350 IBS Implant SystemInnobiosurg Co., Ltd. · 2016
  15. 1 generation backK162099 IBS Implant System IIInnobiosurg Co., Ltd. · 2017
  16. This deviceK200753 IBS Implant System IIInnobiosurg Co., Ltd. · 2020

Most influential descendants

Showing 1 of 1 · See all
  • K220517IBS SystemInnobiosurg Co., Ltd. · 2022 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−15K894595Bonefit R Screw ImplantsInstitut Straumann AG1990—
−14K984104Iti Dental Implant SystemStraumann USA19991
−13K993595Nobel Biocare's Modified Surface Implant (Intended for Immediate Loading Upon…Nobel Biocare Uas, Inc.2000—
−12K0118793A Dental Implant SystemOsseco Biosource, Ltd.2002—
−11K051576Avana Dental Implant SystemOsstem Co., Ltd.2005—
−10K062051SS SystemOsstem Implant Co., Ltd.2006—
−9K063861GS SystemOsstem Implant Co., Ltd.2007—
−8K080744HG II Fixture SystemOsstem Implant Co., Ltd.2008—
−7K082213GS Iii Fixture SystemOsstem Implant Co., Ltd.2008—
−6K093352HG Iii Fixture SystemHiossen, Inc.2009—
−5K101096HT Iii SA Fixture SystemHiossen, Inc.2010—
−4K121585TS Implant SystemOsstem Implant Co., Ltd.2013—
−3K140507Hiossen Prosthetic SystemOsstem Implant Co., Ltd.2014—
−2K153350IBS Implant SystemInnobiosurg Co., Ltd.2016—
−1K162099IBS Implant System IIInnobiosurg Co., Ltd.2017—
0 (this device)K200753IBS Implant System IIInnobiosurg Co., Ltd.2020—
+1K220517IBS SystemInnobiosurg Co., Ltd.2022—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199020
199210
199320
199430
199510
199660
199740
199820
199960
200020
200170
200290
200340
200450
200530
200660
200760
200870
200910
201040
201120
201220
201310
201510

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202210
FIG. 1 — Lineage of K200753, 1990–2022Source: 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 NHA? 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 NHA device

  1. #1 K222288 DESS Dental Smart Solutionsscore 30.6 · 19 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
*K162099IBS Implant System II
Summary page 4
…Class: Class II • Date prepared: 06/09/2020 Predicate Devices: The subject device is substantially equivalent to the following predicate devices: Primary Predicate K162099, IBS Implant System II manufactured by InnoBioSurg Co., Ltd. Indication for Use The IBS Implant System II is intended to replace…
Innobiosurg Co., Ltd.2017—
†K140806Ibs Implant SystemInnobiosurg Co., Ltd.2015—

Also cleared against K162099: 1 other device →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K220517IBS SystemInnobiosurg Co., Ltd.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 30 years and passes through 8 companies; a new generation was cleared every 1.2 years on median.
  • 9 of the 102 ancestors have a recall of any class.
  • Of its descendants, K220517 (Innobiosurg Co., Ltd., 2022) has gone furthest, with 0 descendants of its own.
  • 1 other device also cites its predicate K162099.

How does its category compare?

All NHA devices

NHA Abutment, Implant, Dental, Endosseous: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.

FDA decisions per year · NHA

40in 2025

2007: 382008: 312009: 302010: 192011: 312012: 252013: 222014: 272015: 292016: 382017: 312018: 312019: 282020: 382021: 292022: 332023: 512024: 432025: 402026 (partial year): 23
2007high 51 (2023) · low 19 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NHA

147in 2025

2007: 91 days median2008: 90 days median2009: 95 days median2010: 162 days median2011: 130 days median2012: 171 days median2013: 184 days median2014: 160 days median2015: 151 days median2016: 202 days median2017: 188 days median2018: 200 days median2019: 160 days median2020: 153 days median2021: 211 days median2022: 142 days median2023: 147 days median2024: 158 days median2025: 147 days median2026 (partial year): 169 days median
2007high 211 (2021) · low 90 (2008)2026

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

Recalls per year · NHA

1in 2025

2007: 12008: 22011: 52012: 12013: 12015: 12016: 362017: 22018: 12020: 72023: 32025: 12026 (partial year): 3
2007high 36 (2016) · low 0 (2009)2026

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

Adverse event reports per year · NHA

838in 2025

2007: 12008: 82009: 302010: 612011: 562012: 52013: 1432014: 1462015: 8582016: 3142017: 5772018: 5912019: 5302020: 4582021: 5462022: 4972023: 6182024: 6352025: 838
2007high 858 (2015) · low 1 (2007)2025

MAUDE reports naming product code NHA, 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
2007389111
2008319028
20093095030
201019162061
201131130556
20122517115
2013221841143
2014271600146
2015291511858
20163820236314
2017311882577
2018312001591
2019281600530
2020381537458
2021292110546
2022331420497
2023511473618
2024431580635
2025401471838
2026231693—

What is it indicated for?

The IBS Implant System II is intended to replace missing teeth to restore chewing function. The IBS Implant System II can be placed in support of single or multiple-unit restorations including; cement retained, screw retained, or overdenture restorations, and terminal or immediate abutment support for fixed bridgework. This system is for one or two stage surgical procedures. This system is intended for delayed loading.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K200753: IBS Implant System II.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K200753

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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