510(k) · Cleared
ClearedRelieva Seeker Balloon Sinuplasty System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Acclarent, Inc. · LRC Instrument, Ent Manual Surgical
Cleared on Nov 5, 2012 as substantially equivalent to K111875 (Acclarent, Inc., 2011) and 2 other predicates after a 280-day review. Its family tree reaches back 15 generations to 1994. 2 later devices descend from it.
- Decided
- Nov 5, 2012
- Review
- 280 days
- Class
- Class I
- Product code
- LRC
- Recalls
- None
- Predicates
- 3
Its longest line of descent runs back 15 generations to K936109 (1994). 82 ancestors in all, the oldest K800617 (1980). 2 later devices descend from it, 2 citing it directly.
- Root · 15 generations backK936109 Sharplan Model 1120 CO2 Surgical LaserSharplan Lasers, Inc. · 1994
- 11 generations between
- 3 generations backK093007 Entellus Medical Balloon DeviceEntellus Medical, Inc. · 2010
- 2 generations backK102003 Xpress Balloon DeviceEntellus Medical, Inc. · 2010
- 1 generation backK111875 Relieva Spin Sinus Dilation SystemAcclarent, Inc. · 2011
- This deviceK120280 Relieva Seeker Balloon Sinuplasty SystemAcclarent, Inc. · 2012
- Descendant · cites it directly · 0 of its ownK153341 Relieva Scout Multi-Sinus Dilation SystemAcclarent, Inc. · 2016
- Descendant · cites it directly · 0 of its ownK140160 Relieva Scout Sinus Dilation SystemAcclarent, Inc. · 2014
Show all 15 generations
- Root · 15 generations backK936109 Sharplan Model 1120 CO2 Surgical LaserSharplan Lasers, Inc. · 1994
- 14 generations backK960521 Sharplan Lasers, Inc. Silktouch Flash ScannerSharplan Lasers, Inc. · 1996
- 13 generations backK963339 Coherent Ultrapulse CO2 Surgical LasersCoherent Medical Group · 1997
- 12 generations backK974789 Coherent Ultrapulse S Series CO2 Surgical Lasers Model C and LLumenis, Inc. · 1998
- 11 generations backK990947 Modified Versapulse Select Single Wavelength, HO: Yag and Dual…Lumenis, Inc. · 1999
- 10 generations backK011703 Lumenis Versapulse Powersuite Holmium (HO:Yag) and Dual Wavelength…Lumenis · 2001 · Recalled
- 9 generations backK014290 Entec Plasma WandsArthrocare Corp. · 2002
- 8 generations backK021364 Modification to Entec Plasma WandsArthrocare Corp. · 2002
- 7 generations backK030108 Arthrocare Ent Coblator Surgery SystemArthrocare Corp. · 2003 · Recalled
- 6 generations backK034004 Diego RF Powered Dissector and Drill System ConsoleGyrus Ent LLC · 2004
- 5 generations backK072302 Entellus Medical RS-Series SystemEntellus Medical, Inc. · 2008
- 4 generations backK081542 Modification to Entellus Medical RS-Series SystemEntellus Medical, Inc. · 2008
- 3 generations backK093007 Entellus Medical Balloon DeviceEntellus Medical, Inc. · 2010
- 2 generations backK102003 Xpress Balloon DeviceEntellus Medical, Inc. · 2010
- 1 generation backK111875 Relieva Spin Sinus Dilation SystemAcclarent, Inc. · 2011
- This deviceK120280 Relieva Seeker Balloon Sinuplasty SystemAcclarent, Inc. · 2012
Most influential descendants
Showing 2 of 2 · See allView FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −15 | K936109 | Sharplan Model 1120 CO2 Surgical Laser | Sharplan Lasers, Inc. | 1994 | — |
| −14 | K960521 | Sharplan Lasers, Inc. Silktouch Flash Scanner | Sharplan Lasers, Inc. | 1996 | — |
| −13 | K963339 | Coherent Ultrapulse CO2 Surgical Lasers | Coherent Medical Group | 1997 | — |
| −12 | K974789 | Coherent Ultrapulse S Series CO2 Surgical Lasers Model C and L | Lumenis, Inc. | 1998 | — |
| −11 | K990947 | Modified Versapulse Select Single Wavelength, HO: Yag and Dual Wavelength, HO… | Lumenis, Inc. | 1999 | — |
| −10 | K011703 | Lumenis Versapulse Powersuite Holmium (HO:Yag) and Dual Wavelength… | Lumenis | 2001 | 2 |
| −9 | K014290 | Entec Plasma Wands | Arthrocare Corp. | 2002 | — |
| −8 | K021364 | Modification to Entec Plasma Wands | Arthrocare Corp. | 2002 | — |
| −7 | K030108 | Arthrocare Ent Coblator Surgery System | Arthrocare Corp. | 2003 | 1 |
| −6 | K034004 | Diego RF Powered Dissector and Drill System Console | Gyrus Ent LLC | 2004 | — |
| −5 | K072302 | Entellus Medical RS-Series System | Entellus Medical, Inc. | 2008 | — |
| −4 | K081542 | Modification to Entellus Medical RS-Series System | Entellus Medical, Inc. | 2008 | — |
| −3 | K093007 | Entellus Medical Balloon Device | Entellus Medical, Inc. | 2010 | — |
| −2 | K102003 | Xpress Balloon Device | Entellus Medical, Inc. | 2010 | — |
| −1 | K111875 | Relieva Spin Sinus Dilation System | Acclarent, Inc. | 2011 | — |
| 0 (this device) | K120280 | Relieva Seeker Balloon Sinuplasty System | Acclarent, Inc. | 2012 | — |
| +1 | K153341 | Relieva Scout Multi-Sinus Dilation System | Acclarent, Inc. | 2016 | — |
| +1 | K140160 | Relieva Scout Sinus Dilation System | Acclarent, Inc. | 2014 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1980 | 1 | 0 |
| 1986 | 1 | 0 |
| 1989 | 1 | 0 |
| 1990 | 1 | 0 |
| 1991 | 3 | 0 |
| 1992 | 3 | 0 |
| 1993 | 1 | 0 |
| 1994 | 4 | 0 |
| 1995 | 7 | 0 |
| 1996 | 8 | 0 |
| 1997 | 4 | 0 |
| 1998 | 7 | 0 |
| 1999 | 1 | 0 |
| 2000 | 12 | 0 |
| 2001 | 3 | 0 |
| 2002 | 5 | 0 |
| 2003 | 1 | 0 |
| 2005 | 1 | 0 |
| 2006 | 1 | 0 |
| 2007 | 1 | 0 |
| 2008 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2014 | 1 | 0 |
| 2016 | 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 LRC? 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 LRC device
- #1 K230258 BB 8 Sinus Dilation Kitscore 11.1 · 20 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (3)
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 |
|---|---|---|---|
| * | K111875 | Relieva Spin Sinus Dilation SystemSummary page 1…20 Classification Name: Ear, Nose, and Throat Manual Surgical Instrument Product Code: LRC Predicate Devices: Relieva Spin Sinus Dilation System (K111875) Entellus Medical XprESS Multi-Sinus Dilation Tool (K102003) Relieva Luma Sin… | 2011 |
| * | K102003 | Xpress Balloon DeviceSummary page 1…Code: LRC Predicate Devices: Relieva Spin Sinus Dilation System (K111875) Entellus Medical XprESS Multi-Sinus Dilation Tool (K102003) Relieva Luma Sinus Illumination System (K071845) Device Description: The Relieva Seeker Balloon… | 2010 |
| * | K071845 | Relieva Luma Sinus Illumination System, Model Sis-100ASummary page 1…System (K111875) Entellus Medical XprESS Multi-Sinus Dilation Tool (K102003) Relieva Luma Sinus Illumination System (K071845) Device Description: The Relieva Seeker Balloon Sinuplasty System (Seeker) is an integrated device… | 2007 |
What descends from it? (2)
2 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?
- The line of descent spans 18 years and passes through 8 companies; a new generation was cleared every 1.1 years on median.
- 6 of the 82 ancestors have a recall of any class.
- Of its descendants, K153341 (Acclarent, Inc., 2016) has gone furthest, with 0 descendants of its own.
- 3 other devices also cite its predicate K111875.
How does its category compare?
All LRC devicesLRC Instrument, Ent Manual Surgical: FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.
FDA decisions per year · LRC
1in 2023
2026 to Oct 25, outlined.
Median 510(k) review, days · LRC
131in 2020
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · LRC
1in 2024
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · LRC
44in 2025
MAUDE reports naming product code LRC, 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 | 0 | — | 0 | 1 |
| 2008 | 2 | — | 0 | 0 |
| 2009 | 1 | — | 0 | 8 |
| 2010 | 2 | — | 0 | 11 |
| 2011 | 6 | 106 | 0 | 14 |
| 2012 | 7 | 50 | 0 | 48 |
| 2013 | 7 | 104 | 0 | 53 |
| 2014 | 3 | 29 | 0 | 53 |
| 2015 | 6 | 105 | 0 | 41 |
| 2016 | 3 | 100 | 0 | 39 |
| 2017 | 2 | — | 0 | 32 |
| 2018 | 1 | — | 0 | 42 |
| 2019 | 1 | — | 0 | 19 |
| 2020 | 4 | 131 | 0 | 20 |
| 2021 | 0 | — | 0 | 23 |
| 2022 | 1 | — | 0 | 25 |
| 2023 | 1 | — | 1 | 14 |
| 2024 | 0 | — | 1 | 51 |
| 2025 | 0 | — | 0 | 44 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
For patients aged 18 and older, the Relieva Seeker Balloon Sinuplasty System is intended to provide a means to access the frontal sinus space and to dilate the frontal recess, frontal sinus ostia and spaces within the frontal sinus cavity for diagnostic and therapeutic procedures. In addition, the device is intended to illuminate within and transilluminate across nasal and sinus structures.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K120280 · printed Nov 4, 2026
Cite this page
510(k) Report. “K120280: Relieva Seeker Balloon Sinuplasty System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K120280
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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