510(k) · Cleared
ClearedAtlantis Abutment for Straumann Interface
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Atlantis Components, Inc. · NHA Abutment, Implant, Dental, Endosseous
Cleared on Mar 7, 2005 as substantially equivalent to K981858 (Atlantis Components, Inc., 1999) after a 56-day review. Its family tree reaches back 2 generations to 1994. 5 later devices descend from it.
- Decided
- Mar 7, 2005
- Review
- 56 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. 5 later devices descend from it, 1 citing it directly.
- Root · 2 generations backK931468 Restore Hex Cylinder Endosseous SystemLifecore Biomedical, Inc. · 1994
- 1 generation backK981858 Atlantis Abutment and Atlantis Abutment ScrewAtlantis Components, Inc. · 1999
- This deviceK050052 Atlantis Abutment for Straumann InterfaceAtlantis Components, Inc. · 2005
- Descendant · cites it directly · 4 of its ownK083871 Atlantis Straumann Bone Level Abutment, Atlantis Gemini Straumann…Astra Tech, Inc. · 2009
- Descendant · 2 generations on · 1 of its ownK103234 GC Aadva BO AC AbutmentsGC America, Inc. · 2011
- Descendant · 3 generations on · 0 of its ownK141970 Digitek Titanium AbutmentDigitek Dental Solutions Limited · 2015
- Descendant · 2 generations on · 0 of its ownK130216 Atlantis Straumann Bone Level AbutmentDentsply Implant · 2013
- Descendant · 2 generations on · 0 of its ownK113816 GC Aadva Abutment- Zirconium-BO AC BH SVGC America, Inc. · 2013
Most influential descendants
Showing 5 of 5 · See all- K083871Atlantis Straumann Bone Level Abutment, Atlantis Gemini Straumann Bone Level Abutment…Astra Tech, Inc. · 2009 · cites it directly4descendants
- K103234GC Aadva BO AC AbutmentsGC America, Inc. · 2011 · 2 generations on1descendant
- K141970Digitek Titanium AbutmentDigitek Dental Solutions Limited · 2015 · 3 generations on0descendants
- K130216Atlantis Straumann Bone Level AbutmentDentsply Implant · 2013 · 2 generations on0descendants
- K113816GC Aadva Abutment- Zirconium-BO AC BH SVGC America, Inc. · 2013 · 2 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −2 | K931468 | Restore Hex Cylinder Endosseous System | Lifecore Biomedical, Inc. | 1994 | — |
| −1 | K981858 | Atlantis Abutment and Atlantis Abutment Screw | Atlantis Components, Inc. | 1999 | — |
| 0 (this device) | K050052 | Atlantis Abutment for Straumann Interface | Atlantis Components, Inc. | 2005 | — |
| +1 | K083871 | Atlantis Straumann Bone Level Abutment, Atlantis Gemini Straumann Bone Level… | Astra Tech, Inc. | 2009 | — |
| +2 | K103234 | GC Aadva BO AC Abutments | GC America, Inc. | 2011 | — |
| +3 | K141970 | Digitek Titanium Abutment | Digitek Dental Solutions Limited | 2015 | — |
| +2 | K130216 | Atlantis Straumann Bone Level Abutment | Dentsply Implant | 2013 | — |
| +2 | K113816 | GC Aadva Abutment- Zirconium-BO AC BH SV | GC America, Inc. | 2013 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1995 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2009 | 1 | 0 |
| 2011 | 1 | 0 |
| 2013 | 2 | 0 |
| 2015 | 1 | 0 |
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 K222288 DESS Dental Smart Solutionsscore 30.6 · 19 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the 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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K981858 | Atlantis Abutment and Atlantis Abutment ScrewSummary page 1…is claimed (Predicate Device) Manufacturer Device 510(k) Number ATiantis Components Inc. Atlantis Abutment and K981858 Abutment Screw 4. The devices covered in this submission are abutments which are placed into… | 1999 |
What descends from it? (5)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K083871 | Atlantis Straumann Bone Level Abutment, Atlantis Gemini Straumann Bone Level Abutment… | 2009 | 4 |
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 6.0 years on median.
- None of the 3 ancestors has a recall.
- Of its descendants, K083871 (Astra Tech, Inc., 2009) has gone furthest, with 4 descendants of its own.
- 9 other devices also cite its predicate K981858.
How does its category compare?
All NHA devicesNHA Abutment, Implant, Dental, Endosseous: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · NHA
40in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · NHA
147in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · NHA
1in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · NHA
838in 2025
MAUDE reports naming product code NHA, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 38 | 91 | 1 | 1 |
| 2008 | 31 | 90 | 2 | 8 |
| 2009 | 30 | 95 | 0 | 30 |
| 2010 | 19 | 162 | 0 | 61 |
| 2011 | 31 | 130 | 5 | 56 |
| 2012 | 25 | 171 | 1 | 5 |
| 2013 | 22 | 184 | 1 | 143 |
| 2014 | 27 | 160 | 0 | 146 |
| 2015 | 29 | 151 | 1 | 858 |
| 2016 | 38 | 202 | 36 | 314 |
| 2017 | 31 | 188 | 2 | 577 |
| 2018 | 31 | 200 | 1 | 591 |
| 2019 | 28 | 160 | 0 | 530 |
| 2020 | 38 | 153 | 7 | 458 |
| 2021 | 29 | 211 | 0 | 546 |
| 2022 | 33 | 142 | 0 | 497 |
| 2023 | 51 | 147 | 3 | 618 |
| 2024 | 43 | 158 | 0 | 635 |
| 2025 | 40 | 147 | 1 | 838 |
| 2026 | 23 | 169 | 3 | — |
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.
https://510kreport.com/device/K050052 · printed Nov 5, 2026
Cite this page
510(k) Report. “K050052: Atlantis Abutment for Straumann Interface.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K050052
Report an extraction error
Are you the manufacturer?
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