510(k) · Cleared
ClearedBelun Ring BLR-200 (BLR-200)
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Belun Technology Company Limited · DQA Oximeter
Cleared on Oct 11, 2024 as substantially equivalent to K211407 (Belun Technology Company Limited, 2021) and 1 other predicate after a 289-day review. Its family tree reaches back 7 generations to 2000.
- Decided
- Oct 11, 2024
- Review
- 289 days
- Class
- Class II
- Product code
- DQA
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 7 generations to K001085 (2000). No later device cites it as a predicate yet.
- Root · 7 generations backK001085 Modification to Onyx, Finger Clip Pulse Oximeter, Model 9500Nonin Medical, Inc. · 2000
- 6 generations backK051107 Onyx II Finger Pulse Oximeter, Model 9550Nonin Medical, Inc. · 2005
- 5 generations backK070371 Fingertip Pulse Oximeter MD300CBeijing Choice Electronic Technololgy Co., Ltd. · 2007
- 4 generations backK180174 Belun RingBelun Technology Company Limited · 2018
- 3 generations backK191417 Belun RingBelun Technology Company Limited · 2019
- 2 generations backK211407 Belun Ring BLR-100XBelun Technology Company Limited · 2021
- 1 generation backK221361 circul™ pro RingBodimetrics, LLC · 2023
- This deviceK234110 Belun Ring BLR-200 (BLR-200)Belun Technology Company Limited · 2024
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −7 | K001085 | Modification to Onyx, Finger Clip Pulse Oximeter, Model 9500 | Nonin Medical, Inc. | 2000 | — |
| −6 | K051107 | Onyx II Finger Pulse Oximeter, Model 9550 | Nonin Medical, Inc. | 2005 | — |
| −5 | K070371 | Fingertip Pulse Oximeter MD300C | Beijing Choice Electronic Technololgy Co., Ltd. | 2007 | — |
| −4 | K180174 | Belun Ring | Belun Technology Company Limited | 2018 | — |
| −3 | K191417 | Belun Ring | Belun Technology Company Limited | 2019 | — |
| −2 | K211407 | Belun Ring BLR-100X | Belun Technology Company Limited | 2021 | — |
| −1 | K221361 | circul™ pro Ring | Bodimetrics, LLC | 2023 | — |
| 0 (this device) | K234110 | Belun Ring BLR-200 (BLR-200) | Belun Technology Company Limited | 2024 | — |
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 DQA? 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 DQA device
- #1 K221282 Empatica Health Monitoring Platformscore 20.1 · 38 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (2)
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 |
|---|---|---|---|
| * | K211407 | Belun Ring BLR-100XSummary page 5…ber 870.2700 Product Code DQA I Legally Marketed Predicate Devices 21 CFR 807.92(a)(3) Predicate # Predicate Trade Name (Primary Predicate is listed first) Product Code K211407 Belun Ring BLR-100X DQA K221361 circul™ pro Ring DQA Device Description Summary 21 CFR 807.92(a)(4) Belun Ring BLR-200 consists… | 2021 |
| * | K221361 | circul™ pro RingSummary page 5…Legally Marketed Predicate Devices 21 CFR 807.92(a)(3) Predicate # Predicate Trade Name (Primary Predicate is listed first) Product Code K211407 Belun Ring BLR-100X DQA K221361 circul™ pro Ring DQA Device Description Summary 21 CFR 807.92(a)(4) Belun Ring BLR-200 consists of two parts: a Ring, and a host… | 2023 |
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 24 years and passes through 4 companies; a new generation was cleared every 2.0 years on median.
- None of the 7 ancestors has a recall.
- 1 other device also cites its predicate K211407.
How does its category compare?
All DQA devicesDQA Oximeter: FDA decisions, review times, recalls and adverse event reports over 20 years. 2024, this device’s year, is highlighted.
FDA decisions per year · DQA
15in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · DQA
182in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · DQA
3in 2024
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · DQA
399in 2025
MAUDE reports naming product code DQA, 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 | 20 | 122 | 6 | 325 |
| 2008 | 22 | 97 | 5 | 312 |
| 2009 | 35 | 117 | 29 | 281 |
| 2010 | 29 | 127 | 4 | 185 |
| 2011 | 15 | 195 | 1 | 164 |
| 2012 | 14 | 120 | 0 | 322 |
| 2013 | 15 | 182 | 0 | 468 |
| 2014 | 11 | 175 | 2 | 1,124 |
| 2015 | 13 | 158 | 1 | 2,082 |
| 2016 | 14 | 246 | 0 | 1,775 |
| 2017 | 9 | 200 | 0 | 1,190 |
| 2018 | 18 | 260 | 32 | 694 |
| 2019 | 19 | 158 | 0 | 548 |
| 2020 | 15 | 126 | 0 | 426 |
| 2021 | 10 | 174 | 0 | 553 |
| 2022 | 20 | 265 | 0 | 478 |
| 2023 | 13 | 317 | 0 | 392 |
| 2024 | 14 | 285 | 3 | 545 |
| 2025 | 15 | 182 | 0 | 399 |
| 2026 | 8 | 187 | 0 | — |
What is it indicated for?
Belun Ring BLR-200 is a wireless, non-invasive and stand-alone pulse oximeter intended to be used
for spot-checking and/or continuous data collection and recording of oxygen saturation of arterial
hemoglobin (SpO2) and the pulse rate of adult patients through index finger in hospital and home
environment for up to ten hours, during no motion and motion conditions, and for patients who are
well or poorly perfused. It is not intended for single-use and out-of-hospital transport use and does
ot have alarms.
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/K234110 · printed Nov 5, 2026
Cite this page
510(k) Report. “K234110: Belun Ring BLR-200 (BLR-200).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K234110
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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