510(k) Report

510(k) · Cleared

Cleared

MIS LOCKiT Abutments System, OT-Equators and Ball Attachments

K182228510(k) TraditionalCleared Jan 28, 2019165-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

Mis Implants Technologies, Ltd. · NHA Abutment, Implant, Dental, Endosseous

Cleared on Jan 28, 2019 as substantially equivalent to K163349 (Mis Implants Technologies, Ltd., 2017) and 2 other predicates after a 165-day review. Its family tree reaches back 11 generations to 1990.

Decided
Jan 28, 2019
Review
165 days
Class
Class II
Product code
NHA
Recalls
None
Predicates
3

Its longest line of descent runs back 11 generations to K894595 (1990). 97 ancestors in all, the oldest K781060 (1978). No later device cites it as a predicate yet.

Other ancestors, by year cleared 2018: 1 other ancestor2014: 1 other ancestor2011: 1 other ancestor2008: 1 other ancestor2007: 2 other ancestors2004: 4 other ancestors2009: 3 other ancestors2006: 1 other ancestor2005: 3 other ancestors2003: 5 other ancestors2002: 9 other ancestors1999: 2 other ancestors1998: 3 other ancestors1997: 5 other ancestors1995: 4 other ancestors1988: 1 other ancestor2001: 3 other ancestors1996: 7 other ancestors2000: 3 other ancestors1994: 6 other ancestors1993: 3 other ancestors1990: 4 other ancestors1989: 5 other ancestors1987: 2 other ancestors1986: 2 other ancestors1992: 2 other ancestors1985: 1 other ancestor1982: 1 other ancestor1978: 1 other ancestorReference device: K072878 · Modification to: Locator Implant Anchor · Zest Anchors, Inc. · 2007 · recalledReference device: K173326 · MIS CONNECT Conical Connection Abutment · Mis Implants Technologies, Ltd. · 2018K894595 · 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. · 2000K023113 · Replace Tiunite Endosseous Implant · Nobel Biocare Uas, Inc. · 2002 · recalledK041661 · Nobel Biocare Endosseous Implants · Nobel Biocare Uas, Inc. · 2004K050258 · Groovy Implants · Nobel Biocare AB · 2005 · recalledK061003 · SFB & CFB Implants · Nobel Biocare AB · 2006K071370 · Nobelactive Internal Connection Implant · Nobel Biocare AB · 2007 · recalledK101732 · Astra Tech Implant System · Astra Tech AB · 2011K163349 · MIS V3 Conical Connection Dental Implant System­ · Mis Implants Technologies, Ltd. · 2017K172505 · MIS C1 Narrow Platform Conical Connection Implant System, MIS C1 Wide Platform Conical Connection Abutments · Mis Implants Technologies, Ltd. · 201719801990200020102020
  1. Root · 11 generations backK894595 Bonefit R Screw ImplantsInstitut Straumann AG · 1990
  2. 7 generations between
  3. 3 generations backK101732 Astra Tech Implant SystemAstra Tech AB · 2011
  4. 2 generations backK163349 MIS V3 Conical Connection Dental Implant System­Mis Implants Technologies, Ltd. · 2017
  5. 1 generation backK172505 MIS C1 Narrow Platform Conical Connection Implant System, MIS C1…Mis Implants Technologies, Ltd. · 2017
  6. This deviceK182228 MIS LOCKiT Abutments System, OT-Equators and Ball AttachmentsMis Implants Technologies, Ltd. · 2019
Show all 11 generations
  1. Root · 11 generations backK894595 Bonefit R Screw ImplantsInstitut Straumann AG · 1990
  2. 10 generations backK984104 Iti Dental Implant SystemStraumann USA · 1999 · Recalled
  3. 9 generations backK993595 Nobel Biocare's Modified Surface Implant (Intended for Immediate…Nobel Biocare Uas, Inc. · 2000
  4. 8 generations backK023113 Replace Tiunite Endosseous ImplantNobel Biocare Uas, Inc. · 2002 · Recalled
  5. 7 generations backK041661 Nobel Biocare Endosseous ImplantsNobel Biocare Uas, Inc. · 2004
  6. 6 generations backK050258 Groovy ImplantsNobel Biocare AB · 2005 · Recalled
  7. 5 generations backK061003 SFB & CFB ImplantsNobel Biocare AB · 2006
  8. 4 generations backK071370 Nobelactive Internal Connection ImplantNobel Biocare AB · 2007 · Recalled
  9. 3 generations backK101732 Astra Tech Implant SystemAstra Tech AB · 2011
  10. 2 generations backK163349 MIS V3 Conical Connection Dental Implant System­Mis Implants Technologies, Ltd. · 2017
  11. 1 generation backK172505 MIS C1 Narrow Platform Conical Connection Implant System, MIS C1…Mis Implants Technologies, Ltd. · 2017
  12. This deviceK182228 MIS LOCKiT Abutments System, OT-Equators and Ball AttachmentsMis Implants Technologies, Ltd. · 2019
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−11K894595Bonefit R Screw ImplantsInstitut Straumann AG1990—
−10K984104Iti Dental Implant SystemStraumann USA19991
−9K993595Nobel Biocare's Modified Surface Implant (Intended for Immediate Loading Upon…Nobel Biocare Uas, Inc.2000—
−8K023113Replace Tiunite Endosseous ImplantNobel Biocare Uas, Inc.200227
−7K041661Nobel Biocare Endosseous ImplantsNobel Biocare Uas, Inc.2004—
−6K050258Groovy ImplantsNobel Biocare AB200528
−5K061003SFB & CFB ImplantsNobel Biocare AB2006—
−4K071370Nobelactive Internal Connection ImplantNobel Biocare AB20074
−3K101732Astra Tech Implant SystemAstra Tech AB2011—
−2K163349MIS V3 Conical Connection Dental Implant System­Mis Implants Technologies, Ltd.2017—
−1K172505MIS C1 Narrow Platform Conical Connection Implant System, MIS C1 Wide Platform…Mis Implants Technologies, Ltd.2017—
0 (this device)K182228MIS LOCKiT Abutments System, OT-Equators and Ball AttachmentsMis Implants Technologies, Ltd.2019—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
197810
198210
198510
198620
198720
198810
198950
199040
199220
199330
199460
199540
199670
199750
199830
199920
200030
200130
200290
200350
200440
200530
200610
200720
200810
200930
201110
201410
201810
FIG. 1 — Lineage of K182228, 1990–2019Source: 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 30.7 · 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? (3)

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
*K163349MIS V3 Conical Connection Dental Implant System­
Summary page 4
…Class II Classification Panel: Dental Devices Panel 4. Predicate Device(s) Primary predicate device:  MIS Conical Connection Equators cleared under K163349 Reference devices:  Zest Locator® Implants Attachments cleared under K072878  MIS Conical Connection Equators cle…
Mis Implants Technologies, Ltd.2017—
*K172505MIS C1 Narrow Platform Conical Connection Implant System, MIS C1 Wide Platform Conical…
Summary page 4
…quators cleared under K163349 Reference devices:  Zest Locator® Implants Attachments cleared under K072878  MIS Conical Connection Equators cleared under K172505  MIS Internal Hex Connection Equators cleared under K180282  MIS CONNECT Conical Connection Abutment cleared under K1…
Mis Implants Technologies, Ltd.2017—
*K180282MIS Internal Hex Dental Implant System
Summary page 4
…ocator® Implants Attachments cleared under K072878  MIS Conical Connection Equators cleared under K172505  MIS Internal Hex Connection Equators cleared under K180282  MIS CONNECT Conical Connection Abutment cleared under K173326…
Mis Implants Technologies, Ltd.2018—
†K072878Modification to: Locator Implant AnchorZest Anchors, Inc.20071
†K173326MIS CONNECT Conical Connection AbutmentMis Implants Technologies, Ltd.2018—

Also cleared against K163349: 3 other devices →

What descends from it?

No later submission names this one as a predicate yet.

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 29 years and passes through 6 companies; a new generation was cleared every 1.2 years on median.
  • 13 of the 97 ancestors have a recall of any class.
  • 3 other devices also cite its predicate K163349.

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. 2019, 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?

MIS dental implant systems are intended to be surgically placed in the bone of the upper or lower jaw arches to provide support for prosthetic devices, such as artificial teeth, in order to restore masticatory function. When a one-stage surgical procedure is applied, the implant may be immediately loaded when good primary stability is achieved and the occlusal load is appropriate. Narrow implants (Ø3.3mm & UNO) are indicated for use in surgical and…

Read the full statement (157 words)

MIS dental implant systems are intended to be surgically placed in the bone of the upper or lower jaw arches to provide

support for prosthetic devices, such as artificial teeth, in order to restore masticatory function. When a one-stage surgical

procedure is applied, the implant may be immediately loaded when good primary stability is achieved and the occlusal

load is appropriate.

Narrow implants (Ø3.3mm & UNO) are indicated for use in surgical and restorative applications for placement only in the

mandibular central, lateral incisor and maxillary lateral incisor regions of partially edentulous jaws, to provide support for

prosthetic devices such as artificial teeth. Mandibular central and lateral incisors must be splinted if using two or more

narrow implants adjacent to one another.

The long MIS (18 & 20 mm) implants can be used in a tilted manner.

MIS short implants are to be used only with straight abutments.

M4 short implants are indicated for delayed loading only.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K182228: MIS LOCKiT Abutments System, OT-Equators and Ball Attachments.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K182228

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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