510(k) Report

510(k) · Cleared

Cleared

Endosseous Dental Implant Abutment

K051011510(k) TraditionalCleared Jul 12, 200582-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

Atlantis Components, Inc. · NHA Abutment, Implant, Dental, Endosseous

Cleared on Jul 12, 2005 as substantially equivalent to K981858 (Atlantis Components, Inc., 1999) after an 82-day review. Its family tree reaches back 2 generations to 1994. 1 later device descends from it.

Decided
Jul 12, 2005
Review
82 days
Class
Class II
Product code
NHA
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K931468 (1994). 3 ancestors in all. 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 1995: 1 other ancestor2007: 1 descendant clearedK931468 · Restore Hex Cylinder Endosseous System · Lifecore Biomedical, Inc. · 1994K981858 · Atlantis Abutment and Atlantis Abutment Screw · Atlantis Components, Inc. · 19991990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 1 other ancestor 1 generation forward: 1 descendant K981858 · Atlantis Abutment and Atlantis Abutment Screw · Atlantis Components, Inc. · 1999K931468 · Restore Hex Cylinder Endosseous System · Lifecore Biomedical, Inc. · 19940
  1. Root · 2 generations backK931468 Restore Hex Cylinder Endosseous SystemLifecore Biomedical, Inc. · 1994
  2. 1 generation backK981858 Atlantis Abutment and Atlantis Abutment ScrewAtlantis Components, Inc. · 1999
  3. This deviceK051011 Endosseous Dental Implant AbutmentAtlantis Components, Inc. · 2005
  4. Descendant · cites it directly · 0 of its ownK062197 Atlantis Abutment for 3I Certain Micro Mini; Gemini and Gemini+…Atlantis Components, Inc. · 2007

Most influential descendants

Showing 1 of 1 · See all
  • K062197Atlantis Abutment for 3I Certain Micro Mini; Gemini and Gemini+ AbutmentAtlantis Components, Inc. · 2007 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K931468Restore Hex Cylinder Endosseous SystemLifecore Biomedical, Inc.1994—
−1K981858Atlantis Abutment and Atlantis Abutment ScrewAtlantis Components, Inc.1999—
0 (this device)K051011Endosseous Dental Implant AbutmentAtlantis Components, Inc.2005—
+1K062197Atlantis Abutment for 3I Certain Micro Mini; Gemini and Gemini+ AbutmentAtlantis Components, Inc.2007—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199510

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200710
FIG. 1 — Lineage of K051011, 1994–2007Source: 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
*K981858Atlantis Abutment and Atlantis Abutment Screw
Summary page 1
…Predicate Device) Manufacturer Device I510k Number Atlantis Components Atlantis Abutment and Abutment K981858 Inc. I Screw 4. Description of the Device The devices covered in this submission are abutments whi…
Atlantis Components, Inc.1999—

Also cleared against K981858: 9 other devices →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K062197Atlantis Abutment for 3I Certain Micro Mini; Gemini and Gemini+ AbutmentAtlantis Components, Inc.20070

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 11 years and passes through 2 companies; a new generation was cleared every 6.3 years on median.
  • None of the 3 ancestors has a recall.
  • Of its descendants, K062197 (Atlantis Components, Inc., 2007) has gone furthest, with 0 descendants of its own.
  • 9 other devices also cite its predicate K981858.

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.

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 Atlantis Abutment is intended for use as an accessory to an endosseous implant to support a prosthetic device in a partially or completely edentulous patient. It is intended for use to support single and multiple tooth prosthesis, in the mandible or maxilla. The prosthesis can be cement retained to the abutment. The abutment screw is intended to secure the abutment to the endosseous implant.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K051011: Endosseous Dental Implant Abutment.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K051011

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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