510(k) · Cleared
ClearedDentsply Cavitron Jet Wave Air Polishing Prophylaxis System, Model G125
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Dentsply Intl. · EFB Handpiece, Air-Powered, Dental
Cleared on Jun 16, 2004 as substantially equivalent to K900709 (Electro Medical Systems (Ems Sa), 1990) and 1 other predicate after a 47-day review. Its family tree reaches back 1 generation to 1990.
- Decided
- Jun 16, 2004
- Review
- 47 days
- Class
- Class I
- Product code
- EFB
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 1 generation to K900709 (1990). 2 ancestors in all. No later device cites it as a predicate yet.
- Root · 1 generation backK900709 Air Flow SiiElectro Medical Systems (Ems Sa) · 1990
- This deviceK041141 Dentsply Cavitron Jet Wave Air Polishing Prophylaxis System, Model…Dentsply Intl. · 2004
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K900709 | Air Flow Sii | Electro Medical Systems (Ems Sa) | 1990 | — |
| 0 (this device) | K041141 | Dentsply Cavitron Jet Wave Air Polishing Prophylaxis System, Model G125 | Dentsply Intl. | 2004 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1997 | 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 EFB? 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 EFB device
- #1 K262144 DIAMED Handpiece;DIAMED Airmotor;DIAMED…score 13.3 · 5 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 |
|---|---|---|---|
| * | K900709 | Air Flow SiiSummary page 1…ece Classification Name: Dental handpiece and accessories 3. PREDICATE DEVICES * AirFlow S11 (K900709) * Prophyflex 2, Model 2012 (K973876) 4. DEVICE DESCRIPTION… | 1990 |
| * | K973876 | Prophyflex 2, Model 2012Summary page 1…ce and accessories 3. PREDICATE DEVICES * AirFlow S11 (K900709) * Prophyflex 2, Model 2012 (K973876) 4. DEVICE DESCRIPTION… | 1997 |
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?
- None of the 2 ancestors has a recall.
- 3 other devices also cite its predicate K900709.
How does its category compare?
All EFB devicesEFB Handpiece, Air-Powered, Dental: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · EFB
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · EFB
209in 2024
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · EFB
No recall names EFB since 2007.
Adverse event reports per year · EFB
83in 2025
MAUDE reports naming product code EFB, 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 | 12 | 61 | 0 | 13 |
| 2008 | 7 | 97 | 0 | 19 |
| 2009 | 11 | 120 | 0 | 40 |
| 2010 | 8 | 116 | 0 | 78 |
| 2011 | 4 | 168 | 0 | 96 |
| 2012 | 8 | 130 | 0 | 97 |
| 2013 | 3 | 207 | 0 | 61 |
| 2014 | 7 | 200 | 0 | 73 |
| 2015 | 7 | 296 | 0 | 87 |
| 2016 | 3 | 205 | 0 | 122 |
| 2017 | 7 | 246 | 0 | 153 |
| 2018 | 3 | 210 | 0 | 81 |
| 2019 | 3 | 348 | 0 | 117 |
| 2020 | 5 | 259 | 0 | 94 |
| 2021 | 2 | — | 0 | 123 |
| 2022 | 5 | 430 | 0 | 157 |
| 2023 | 4 | 158 | 0 | 116 |
| 2024 | 5 | 209 | 0 | 104 |
| 2025 | 1 | — | 0 | 83 |
| 2026 | 4 | 252 | 0 | — |
What is it indicated for?
The SET WAVETM SYSTEM is indicated for air polishing procedures including the removal of a variety of extrinsic stains; general prophylaxis; and cleaning tooth surfaces prior to bonding and sealant procedures.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K041141 · printed Nov 5, 2026
Cite this page
510(k) Report. “K041141: Dentsply Cavitron Jet Wave Air Polishing Prophylaxis System, Model G125.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K041141
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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