510(k) · Cleared
ClearedOEC One
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Ge Hualun Medical Systems Co., Ltd. · OWB Interventional Fluoroscopic X-Ray System
Cleared on Nov 9, 2017 as substantially equivalent to K123603 (Ge Healthcare Surgery GE Oec Medical Systems, Inc., 2013) after a 63-day review. Its family tree reaches back 6 generations to 2002. 2 of the 11 devices in its family, counting itself, have a Class I recall. 3 later devices descend from it.
- Decided
- Nov 9, 2017
- Review
- 63 days
- Class
- Class II
- Product code
- OWB
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 6 generations to K021049 (2002). 7 ancestors in all. 3 later devices descend from it, 1 citing it directly. 2 of the 11 devices in this family, counting this one, have a Class I recall.
- Root · 6 generations backK021049 Oec 9800 Plus Digital Mobile Imaging SystemGe Oec Medical Systems · 2002 · Recalled (Class I)
- 5 generations backK041932 Oec Olympus Fluoroscopic Imaging SystemGe Oec Medical Systems, Inc. · 2004 · Recalled
- 4 generations backK073543 Oec 9900 EliteGe Oec Medical Systems · 2008 · Recalled
- 3 generations backK082781 Oec 9900 EliteGe Healthcare Surgery · 2009 · Recalled
- 2 generations backK111551 Oec (R) 9800, Oec (R) 9800 PlusGe Oec Medical Systems, Inc. · 2011 · Recalled
- 1 generation backK123603 Oec Brivo 865 Advance, Oec Brivo 785 Essential, and Oec Brivo 715…Ge Healthcare Surgery GE Oec Medical Systems, Inc. · 2013 · Recalled
- This deviceK172700 OEC OneGe Hualun Medical Systems Co., Ltd. · 2017
- Descendant · cites it directly · 2 of its ownK182626 OEC OneGe Hualun Medical Systems Co., Ltd. · 2018
- Descendant · 2 generations on · 1 of its ownK240828 OEC One ASDGe Hualun Medical Systems Co., Ltd. · 2024
- Descendant · 3 generations on · 0 of its ownK253269 OEC One CFDGe Hualun Medical Systems Co., Ltd. · 2025
Class I recalls in this family
Most influential descendants
Showing 3 of 3 · See allView FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −6 | K021049 | Oec 9800 Plus Digital Mobile Imaging System | Ge Oec Medical Systems | 2002 | Class I |
| −5 | K041932 | Oec Olympus Fluoroscopic Imaging System | Ge Oec Medical Systems, Inc. | 2004 | 7 |
| −4 | K073543 | Oec 9900 Elite | Ge Oec Medical Systems | 2008 | 5 |
| −3 | K082781 | Oec 9900 Elite | Ge Healthcare Surgery | 2009 | 4 |
| −2 | K111551 | Oec (R) 9800, Oec (R) 9800 Plus | Ge Oec Medical Systems, Inc. | 2011 | 9 |
| −1 | K123603 | Oec Brivo 865 Advance, Oec Brivo 785 Essential, and Oec Brivo 715 Prime | Ge Healthcare Surgery GE Oec Medical Systems, Inc. | 2013 | 5 |
| 0 (this device) | K172700 | OEC One | Ge Hualun Medical Systems Co., Ltd. | 2017 | — |
| +1 | K182626 | OEC One | Ge Hualun Medical Systems Co., Ltd. | 2018 | — |
| +2 | K240828 | OEC One ASD | Ge Hualun Medical Systems Co., Ltd. | 2024 | — |
| +3 | K253269 | OEC One CFD | Ge Hualun Medical Systems Co., Ltd. | 2025 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2003 | 1 | 1 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2018 | 1 | 0 |
| 2024 | 1 | 0 |
| 2025 | 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.
2 devices in this family have a Class I recall. 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 OWB device
- #1 K251602 Alphenix, INFX-8000V/B, INFX-8000V/S, V9.6…score 18.2 · 18 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 |
|---|---|---|---|
| * | K123603 | Oec Brivo 865 Advance, Oec Brivo 785 Essential, and Oec Brivo 715 PrimeSummary page 4…Class II Classification regulation: 21CFR 892.1650 Primary Product Code: OXO Secondary Product Code: JAA, OWB Predicate Device(s): K123603 OEC Brivo, 892.1650, OXO Device Description: The OEC One™ is a mobile C-arm x-ray system to provide… | 2013 |
What descends from it? (3)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K182626 | OEC One | 2018 | 2 |
Has anything in its family been recalled? (2 Class I)
No FDA recall names this device.
Relatives with a Class I recall
Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.
- K024012Oec 9800 E/CV+ Digital Mobile Imaging SystemGe Oec Medical Systems · 2003 · 5 generations back · ◆ in the 2003 ancestors bar of FIG. 11 Class I recall
- K021049Oec 9800 Plus Digital Mobile Imaging SystemGe Oec Medical Systems · 2002 · 5 generations back · ◆ on the line of descent in FIG. 11 Class I recall
What does this lineage say?
- The line of descent spans 15 years and passes through 5 companies; a new generation was cleared every 2.4 years on median.
- 7 of the 7 ancestors have a recall of any class; 2 have a Class I recall.
- Of its descendants, K182626 (Ge Hualun Medical Systems Co., Ltd., 2018) has gone furthest, with 2 descendants of its own.
How does its category compare?
All OWB devicesOWB Interventional Fluoroscopic X-Ray System: FDA decisions, review times, recalls and adverse event reports over 20 years. 2017, this device’s year, is highlighted.
FDA decisions per year · OWB
22in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · OWB
148in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · OWB
42so far in 2026, the most since 2007
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · OWB
14,008in 2025
MAUDE reports naming product code OWB, 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 | 3 | 52 | 0 | 1 |
| 2008 | 4 | 135 | 1 | 0 |
| 2009 | 9 | 99 | 0 | 0 |
| 2010 | 7 | 66 | 0 | 0 |
| 2011 | 6 | 79 | 0 | 1 |
| 2012 | 6 | 37 | 0 | 1 |
| 2013 | 11 | 119 | 10 | 27 |
| 2014 | 15 | 158 | 9 | 103 |
| 2015 | 11 | 66 | 35 | 2,134 |
| 2016 | 16 | 103 | 13 | 4,074 |
| 2017 | 20 | 76 | 13 | 1,604 |
| 2018 | 23 | 54 | 6 | 1,449 |
| 2019 | 9 | 174 | 7 | 1,558 |
| 2020 | 16 | 53 | 8 | 1,581 |
| 2021 | 24 | 60 | 31 | 1,981 |
| 2022 | 21 | 90 | 24 | 2,932 |
| 2023 | 12 | 152 | 22 | 7,604 |
| 2024 | 13 | 126 | 11 | 7,942 |
| 2025 | 22 | 148 | 30 | 14,008 |
| 2026 | 15 | 221 | 42 | — |
What is it indicated for?
The OEC One mobile C-arm system is designed to provide fluoroscopic and digital spot/film images of adult and pediatric patient populations during diagnostic, interventional, and surgical procedures. Examples of a clinical application may include: orthopedic, gastrointestinal, endoscopic, urologic, neurologic, critical care, and emergency procedures.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K172700 · printed Nov 6, 2026
Cite this page
510(k) Report. “K172700: OEC One.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K172700
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