510(k) Report

510(k) · Cleared

Cleared

Scarlet SRF

K180872510(k) TraditionalCleared Oct 11, 2018191-day reviewClass II21 CFR 878.4400

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

VIOL Co., Ltd. · GEI Electrosurgical, Cutting & Coagulation & Accessories

Cleared on Oct 11, 2018 as substantially equivalent to K121481 (Lutronic Corporation, 2013) after a 191-day review. Its family tree reaches back 11 generations to 1995. 4 later devices descend from it.

Decided
Oct 11, 2018
Review
191 days
Class
Class II
Product code
GEI
Recalls
None
Predicates
1

Its longest line of descent runs back 11 generations to K943450 (1995). 24 ancestors in all, the oldest K800617 (1980). 4 later devices descend from it, 2 citing it directly.

  1. Root · 11 generations backK943450 Arthrocare Arthroscopic Electrosurgery System Model 970Arthrocare Corp. · 1995
  2. 7 generations between
  3. 3 generations backK080145 Primaeva Medical SystemPrimaeva Medical, Inc. · 2008
  4. 2 generations backK082391 Primaeva Medical Renesis SystemPrimaeva Medical, Inc. · 2009
  5. 1 generation backK121481 Infini Radiofrequency SystemLutronic Corporation · 2013
  6. This deviceK180872 Scarlet SRFVIOL Co., Ltd. · 2018
  7. Descendant · cites it directly · 2 of its ownK200185 Sylfirm XVIOL Co., Ltd. · 2020
  8. Descendant · 2 generations on · 1 of its ownK213612 Sylfirm XVIOL Co., Ltd. · 2022
  9. Descendant · cites it directly · 0 of its ownK253859 Scarlet Pro (Scarlet Pro)VIOL Co., Ltd. · 2026
  10. Descendant · 3 generations on · 0 of its ownK243097 RM STAR EX with RMS NeedleBomtech Electronics Co., Ltd. · 2024
Show all 11 generations
  1. Root · 11 generations backK943450 Arthrocare Arthroscopic Electrosurgery System Model 970Arthrocare Corp. · 1995
  2. 10 generations backK961069 Arthrocare Urologic Multi-Electrode Electrosurgery SystemArthrocare Corp. · 1996
  3. 9 generations backK962445 Arthrocare Dental Electrosurgery SystemArthrocare Corp. · 1996
  4. 8 generations backK964849 Arthrocare Dermatologic Electrosurgery SystemArthrocare Corp. · 1997
  5. 7 generations backK973478 Arthrocare Sinus Electrosurgery SystemArthrocare Corp. · 1998
  6. 6 generations backK981870 Visage Cosmetic Surgery SystemArthrocare Corp. · 1998
  7. 5 generations backK000944 Thermage Thermacool SystemThermage, Inc. · 2000
  8. 4 generations backK072261 Finesse SystemPrimaeva Medical, Inc. · 2007
  9. 3 generations backK080145 Primaeva Medical SystemPrimaeva Medical, Inc. · 2008
  10. 2 generations backK082391 Primaeva Medical Renesis SystemPrimaeva Medical, Inc. · 2009
  11. 1 generation backK121481 Infini Radiofrequency SystemLutronic Corporation · 2013
  12. This deviceK180872 Scarlet SRFVIOL Co., Ltd. · 2018

Most influential descendants

Showing 4 of 4 · See all
  • K200185Sylfirm XVIOL Co., Ltd. · 2020 · cites it directly2descendants
  • K213612Sylfirm XVIOL Co., Ltd. · 2022 · 2 generations on1descendant
  • K253859Scarlet Pro (Scarlet Pro)VIOL Co., Ltd. · 2026 · cites it directly0descendants
  • K243097RM STAR EX with RMS NeedleBomtech Electronics Co., Ltd. · 2024 · 3 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−11K943450Arthrocare Arthroscopic Electrosurgery System Model 970Arthrocare Corp.1995—
−10K961069Arthrocare Urologic Multi-Electrode Electrosurgery SystemArthrocare Corp.1996—
−9K962445Arthrocare Dental Electrosurgery SystemArthrocare Corp.1996—
−8K964849Arthrocare Dermatologic Electrosurgery SystemArthrocare Corp.1997—
−7K973478Arthrocare Sinus Electrosurgery SystemArthrocare Corp.1998—
−6K981870Visage Cosmetic Surgery SystemArthrocare Corp.1998—
−5K000944Thermage Thermacool SystemThermage, Inc.2000—
−4K072261Finesse SystemPrimaeva Medical, Inc.2007—
−3K080145Primaeva Medical SystemPrimaeva Medical, Inc.2008—
−2K082391Primaeva Medical Renesis SystemPrimaeva Medical, Inc.2009—
−1K121481Infini Radiofrequency SystemLutronic Corporation2013—
0 (this device)K180872Scarlet SRFVIOL Co., Ltd.2018—
+1K200185Sylfirm XVIOL Co., Ltd.2020—
+2K213612Sylfirm XVIOL Co., Ltd.2022—
+1K253859Scarlet Pro (Scarlet Pro)VIOL Co., Ltd.2026—
+3K243097RM STAR EX with RMS NeedleBomtech Electronics Co., Ltd.2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198010
199220
199410
199520
199650
199910
200010

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202010
202210
202410
202610
FIG. 1 — Lineage of K180872, 1995–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

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 GEI? 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 GEI device

  1. #1 K231790 The InMode System with the Morpheus8 Applicatorsscore 32.7 · 21 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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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.

TypeNumberDeviceApplicantDecidedRecalls
*K121481Infini Radiofrequency System
Summary page 4
…e devices Applicant Device Name 510(k) Number Lutronic Corporation INFINI Radiofrequency System K121481 1…
Lutronic Corporation2013—
†K150409VIVACE Electrosurgical SystemSung Hwan E&B Co.,Ltd20161

Also cleared against K121481: 8 other devices →

What descends from it? (4)

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K200185Sylfirm XVIOL Co., Ltd.20202
K253859Scarlet Pro (Scarlet Pro)VIOL Co., Ltd.20260

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 23 years and passes through 5 companies; a new generation was cleared every 1.2 years on median.
  • 2 of the 24 ancestors have a recall of any class.
  • Of its descendants, K200185 (VIOL Co., Ltd., 2020) has gone furthest, with 2 descendants of its own.
  • 8 other devices also cite its predicate K121481.

How does its category compare?

All GEI devices

GEI Electrosurgical, Cutting & Coagulation & Accessories: FDA decisions, review times, recalls and adverse event reports over 20 years. 2018, this device’s year, is highlighted.

FDA decisions per year · GEI

52in 2025

2007: 502008: 612009: 422010: 462011: 352012: 392013: 482014: 492015: 472016: 642017: 522018: 472019: 482020: 592021: 462022: 552023: 652024: 592025: 522026 (partial year): 43
2007high 65 (2023) · low 35 (2011)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GEI

113in 2025

2007: 51 days median2008: 71 days median2009: 130 days median2010: 109 days median2011: 135 days median2012: 133 days median2013: 136 days median2014: 103 days median2015: 123 days median2016: 108 days median2017: 72 days median2018: 93 days median2019: 93 days median2020: 105 days median2021: 146 days median2022: 150 days median2023: 104 days median2024: 125 days median2025: 113 days median2026 (partial year): 183 days median
2007high 183 (2026) · low 51 (2007)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · GEI

4in 2025

2007: 212008: 192009: 272010: 512011: 322012: 302013: 132014: 32015: 42016: 32017: 22018: 62019: 52020: 12021: 62022: 492023: 27, 4 Class I2024: 22, 10 Class I2025: 42026 (partial year): 8
2007high 51 (2010) · low 1 (2020)2026

Class I (14 since 2007) Class II/III not classified

Adverse event reports per year · GEI

7,592in 2025

2007: 2,7952008: 2,5562009: 3,5912010: 3,3772011: 4,4632012: 5,2162013: 4,8972014: 4,9082015: 4,9362016: 5,6162017: 6,0732018: 6,5452019: 7,0672020: 6,4902021: 6,3542022: 6,1032023: 7,1762024: 7,8972025: 7,592
2007high 7,897 (2024) · low 2,556 (2008)2025

MAUDE reports naming product code GEI, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20075051212,795
20086171192,556
200942130273,591
201046109513,377
201135135324,463
201239133305,216
201348136134,897
20144910334,908
20154712344,936
20166410835,616
2017527226,073
2018479366,545
2019489357,067
20205910516,490
20214614666,354
202255150496,103
20236510427 (4)7,176
20245912522 (10)7,897
20255211347,592
2026431838—

What is it indicated for?

The SCARLET SRF is intended for use in dermatologic and general surgical procedures for electrocoagulation and hemostasis.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K180872: Scarlet SRF.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K180872

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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