510(k) · Cleared
ClearedDynasty Acetabular System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Wrightmedicaltechnologyinc · JDL Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)
Cleared on Jul 11, 2007 after a 112-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 17 later devices descend from it.
- Decided
- Jul 11, 2007
- Review
- 112 days
- Class
- Class III
- Product code
- JDL
- Recalls
- None
- Predicates
- 0
17 later devices descend from it, 4 citing it directly.
- This deviceK070785 Dynasty Acetabular SystemWrightmedicaltechnologyinc · 2007
- Descendant · cites it directly · 16 of its ownK170444 PROCOTYL® PRIME Acetabular Cup SystemMicroport Orthopedics, Inc. · 2017
- Descendant · cites it directly · 10 of its ownK171181 PROCOTYL® PRIME E-CLASS™ XLPE LinerMicroport Orthopedics, Inc. · 2017
- Descendant · 2 generations on · 5 of its ownK180263 EcoFit Vit E Acetabular SystemImplantcast GmbH · 2018
- Descendant · 3 generations on · 4 of its ownK203420 EcoFit® Hip SystemImplantcast GmbH · 2021
- Descendant · 2 generations on · 2 of its ownK180798 Prime Acetabular Cup SystemMicroport Orthopedics, Inc. · 2018
Showing 5 of 17 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 17 · See all- K170444PROCOTYL® PRIME Acetabular Cup SystemMicroport Orthopedics, Inc. · 2017 · cites it directly16descendants
- K171181PROCOTYL® PRIME E-CLASS™ XLPE LinerMicroport Orthopedics, Inc. · 2017 · cites it directly10descendants
- K180263EcoFit Vit E Acetabular SystemImplantcast GmbH · 2018 · 2 generations on5descendants
- K203420EcoFit® Hip SystemImplantcast GmbH · 2021 · 3 generations on4descendants
- K180798Prime Acetabular Cup SystemMicroport Orthopedics, Inc. · 2018 · 2 generations on2descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K070785 | Dynasty Acetabular System | Wrightmedicaltechnologyinc | 2007 | — |
| +1 | K170444 | PROCOTYL® PRIME Acetabular Cup System | Microport Orthopedics, Inc. | 2017 | — |
| +1 | K171181 | PROCOTYL® PRIME E-CLASS™ XLPE Liner | Microport Orthopedics, Inc. | 2017 | — |
| +2 | K180263 | EcoFit Vit E Acetabular System | Implantcast GmbH | 2018 | — |
| +3 | K203420 | EcoFit® Hip System | Implantcast GmbH | 2021 | — |
| +2 | K180798 | Prime Acetabular Cup System | Microport Orthopedics, Inc. | 2018 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2017 | 2 | 0 |
| 2018 | 4 | 0 |
| 2019 | 1 | 0 |
| 2021 | 3 | 0 |
| 2022 | 1 | 0 |
| 2023 | 1 | 0 |
| 2024 | 3 | 0 |
| 2026 | 2 | 0 |
Sources: FDA 510(k) database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in JDL? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
- Candidate predicates for a device like this, rankedin the report
- Recall history across each candidate’s familyin the report
What was it cleared against?
FDA has not posted a summary or statement for it, so its predicates are not known.
What descends from it? (17)
See all 174 later devices cite it directly; ranked here by how many devices descend from each in turn.
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?
- Of its descendants, K170444 (Microport Orthopedics, Inc., 2017) has gone furthest, with 16 descendants of its own.
How does its category compare?
All JDL devicesJDL Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component): FDA decisions, review times, recalls and adverse event reports over 20 years. 2007, this device’s year, is highlighted.
FDA decisions per year · JDL
1in 2008
2026 to Oct 25, outlined.
Median 510(k) review, days · JDL
Too few JDL 510(k)s in any year since 2007 to give a median.
Recalls per year · JDL
1in 2010
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · JDL
16in 2025
MAUDE reports naming product code JDL, 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 | 1 | — | 0 | 79 |
| 2008 | 1 | — | 0 | 67 |
| 2009 | 0 | — | 2 | 104 |
| 2010 | 0 | — | 1 | 198 |
| 2011 | 0 | — | 0 | 271 |
| 2012 | 0 | — | 0 | 338 |
| 2013 | 0 | — | 0 | 496 |
| 2014 | 0 | — | 0 | 519 |
| 2015 | 0 | — | 0 | 466 |
| 2016 | 0 | — | 0 | 299 |
| 2017 | 0 | — | 0 | 336 |
| 2018 | 0 | — | 0 | 205 |
| 2019 | 0 | — | 0 | 140 |
| 2020 | 0 | — | 0 | 94 |
| 2021 | 0 | — | 0 | 68 |
| 2022 | 0 | — | 0 | 49 |
| 2023 | 0 | — | 0 | 32 |
| 2024 | 0 | — | 0 | 27 |
| 2025 | 0 | — | 0 | 16 |
| 2026 | 0 | — | 1 | — |
https://510kreport.com/device/K070785 · printed Nov 6, 2026
Cite this page
510(k) Report. “K070785: Dynasty Acetabular System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K070785
Report an extraction error
Are you the manufacturer?
Record history
- FDA decision record loaded May 2, 2026
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026