510(k) Report

510(k) · Cleared

Cleared

10PL

K220794510(k) TraditionalCleared Nov 10, 2022237-day reviewClass II21 CFR 878.4810

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

Tentech Co., Ltd. · ONF Powered Light Based Non-Laser Surgical Instrument With Thermal Effect

Cleared on Nov 10, 2022 as substantially equivalent to K102857 (Ahwon Medi Instrument Co., Ltd., 2011) and 2 other predicates after a 237-day review. Its family tree reaches back 23 generations to 1995.

Decided
Nov 10, 2022
Review
237 days
Class
Class II
Product code
ONF
Recalls
None
Predicates
3

Its longest line of descent runs back 23 generations to K943450 (1995). 570 ancestors in all, the oldest K771218 (1978). No later device cites it as a predicate yet.

Other ancestors, by year cleared 2018: 1 other ancestor2011: 8 other ancestors2015: 2 other ancestors2009: 14 other ancestors2008: 21 other ancestors2002: 45 other ancestors2013: 2 other ancestors2006: 20 other ancestors2005: 32 other ancestors2004: 38 other ancestors2003: 50 other ancestors2001: 34 other ancestors1998: 31 other ancestors2000: 35 other ancestors1999: 27 other ancestors1997: 31 other ancestors1996: 30 other ancestors1995: 27 other ancestors1994: 25 other ancestors2010: 3 other ancestors2007: 18 other ancestors1993: 12 other ancestors1991: 10 other ancestors1990: 7 other ancestors1989: 4 other ancestors1992: 5 other ancestors1986: 2 other ancestors1984: 1 other ancestor1982: 2 other ancestors1980: 1 other ancestor1988: 4 other ancestors1985: 1 other ancestor1987: 2 other ancestors1981: 1 other ancestor1978: 1 other ancestorK943450 · Arthrocare Arthroscopic Electrosurgery System Model 970 · Arthrocare Corp. · 1995×2: 2 generations cleared close together, K961069 (1996), K962445 (1996) K964849 · Arthrocare Dermatologic Electrosurgery System · Arthrocare Corp. · 1997K973478 · Arthrocare Sinus Electrosurgery System · Arthrocare Corp. · 1998K981870 · Visage Cosmetic Surgery System · Arthrocare Corp. · 1998K000944 · Thermage Thermacool System · Thermage, Inc. · 2000×2: 2 generations cleared close together, K013034 (2001), K013639 (2002) ×2: 2 generations cleared close together, K021402 (2002), K030142 (2003) K031671 · Polaris WR · Syneron Medical, Ltd. · 2003K041959 · Polaris DS/Comet · Syneron Medical, Ltd. · 2004K053540 · Intermedic Diode Laser Family 810NM and 980NM (and the Delivery Accessories That Are Used with Them to Deliver Laser Ene · Intermedic Arfran, SA · 2006×2: 2 generations cleared close together, K071295 (2007), K072106 (2007) K083682 · 180W Cerelas D 980NM Diode Laser, Model D180 · Biolitec, Inc. · 2009K082230 · Vectra Plus Laser System and Accessories · Xintec Corporation · 2010K101916 · Joule Multi-Platform System · Sciton, Inc · 2011K140009 · Soprano Ice Multi-Application & Multi-Technology Platform · Alma Lasers, Ltd. · 2014K143519 · The MeDioStar NeXT Family · Asclepion Laser Technologies GmbH · 2015K152714 · Quanta Forte · Quanta System Spa · 2015K192539 · Deka Luxea · El.En Electronic Engineering Spa · 201919801990200020102020
Other ancestors, by generation 1 generation back: 2 other ancestors2 generations back: 7 other ancestors3 generations back: 35 other ancestors4 generations back: 90 other ancestors5 generations back: 87 other ancestors6 generations back: 73 other ancestors7 generations back: 90 other ancestors8 generations back: 84 other ancestors9 generations back: 57 other ancestors10 generations back: 19 other ancestors11 generations back: 3 other ancestors K192539 · Deka Luxea · El.En Electronic Engineering Spa · 2019K152714 · Quanta Forte · Quanta System Spa · 2015K143519 · The MeDioStar NeXT Family · Asclepion Laser Technologies GmbH · 2015K140009 · Soprano Ice Multi-Application & Multi-Technology Platform · Alma Lasers, Ltd. · 2014K101916 · Joule Multi-Platform System · Sciton, Inc · 2011K082230 · Vectra Plus Laser System and Accessories · Xintec Corporation · 2010K083682 · 180W Cerelas D 980NM Diode Laser, Model D180 · Biolitec, Inc. · 2009K072106 · 150W Ceralas D 980NM Diode Laser · Biolitec, Inc. · 2007K071295 · 100W Ceralas D 980NM Diode Laser · Biolitec, Inc. · 2007K053540 · Intermedic Diode Laser Family 810NM and 980NM (and the Delivery Accessories That Are Used with Them to Deliver Laser Ene · Intermedic Arfran, SA · 2006K041959 · Polaris DS/Comet · Syneron Medical, Ltd. · 2004K031671 · Polaris WR · Syneron Medical, Ltd. · 2003K030142 · Thermacool TC System · Thermage, Inc. · 2003K021402 · Thermage Thermacool TC System · Thermage, Inc. · 2002K013639 · Thermage Thermacool TC System · Thermage, Inc. · 2002K013034 · Modification to: Thermacool Iia · Thermage, Inc. · 2001K000944 · Thermage Thermacool System · Thermage, Inc. · 2000K981870 · Visage Cosmetic Surgery System · Arthrocare Corp. · 1998K973478 · Arthrocare Sinus Electrosurgery System · Arthrocare Corp. · 1998K964849 · Arthrocare Dermatologic Electrosurgery System · Arthrocare Corp. · 1997K962445 · Arthrocare Dental Electrosurgery System · Arthrocare Corp. · 1996K961069 · Arthrocare Urologic Multi-Electrode Electrosurgery System · Arthrocare Corp. · 1996K943450 · Arthrocare Arthroscopic Electrosurgery System Model 970 · Arthrocare Corp. · 1995−20−15−10−50
  1. Root · 23 generations backK943450 Arthrocare Arthroscopic Electrosurgery System Model 970Arthrocare Corp. · 1995
  2. 19 generations between
  3. 3 generations backK143519 The MeDioStar NeXT FamilyAsclepion Laser Technologies GmbH · 2015
  4. 2 generations backK152714 Quanta ForteQuanta System Spa · 2015
  5. 1 generation backK192539 Deka LuxeaEl.En Electronic Engineering Spa · 2019
  6. This deviceK220794 10PLTentech Co., Ltd. · 2022
Show all 23 generations
  1. Root · 23 generations backK943450 Arthrocare Arthroscopic Electrosurgery System Model 970Arthrocare Corp. · 1995
  2. 22 generations backK961069 Arthrocare Urologic Multi-Electrode Electrosurgery SystemArthrocare Corp. · 1996
  3. 21 generations backK962445 Arthrocare Dental Electrosurgery SystemArthrocare Corp. · 1996
  4. 20 generations backK964849 Arthrocare Dermatologic Electrosurgery SystemArthrocare Corp. · 1997
  5. 19 generations backK973478 Arthrocare Sinus Electrosurgery SystemArthrocare Corp. · 1998
  6. 18 generations backK981870 Visage Cosmetic Surgery SystemArthrocare Corp. · 1998
  7. 17 generations backK000944 Thermage Thermacool SystemThermage, Inc. · 2000
  8. 16 generations backK013034 Modification to: Thermacool IiaThermage, Inc. · 2001
  9. 15 generations backK013639 Thermage Thermacool TC SystemThermage, Inc. · 2002
  10. 14 generations backK021402 Thermage Thermacool TC SystemThermage, Inc. · 2002
  11. 13 generations backK030142 Thermacool TC SystemThermage, Inc. · 2003
  12. 12 generations backK031671 Polaris WRSyneron Medical, Ltd. · 2003
  13. 11 generations backK041959 Polaris DS/CometSyneron Medical, Ltd. · 2004
  14. 10 generations backK053540 Intermedic Diode Laser Family 810NM and 980NM (and the Delivery…Intermedic Arfran, SA · 2006
  15. 9 generations backK071295 100W Ceralas D 980NM Diode LaserBiolitec, Inc. · 2007
  16. 8 generations backK072106 150W Ceralas D 980NM Diode LaserBiolitec, Inc. · 2007
  17. 7 generations backK083682 180W Cerelas D 980NM Diode Laser, Model D180Biolitec, Inc. · 2009
  18. 6 generations backK082230 Vectra Plus Laser System and AccessoriesXintec Corporation · 2010
  19. 5 generations backK101916 Joule Multi-Platform SystemSciton, Inc · 2011
  20. 4 generations backK140009 Soprano Ice Multi-Application & Multi-Technology PlatformAlma Lasers, Ltd. · 2014
  21. 3 generations backK143519 The MeDioStar NeXT FamilyAsclepion Laser Technologies GmbH · 2015
  22. 2 generations backK152714 Quanta ForteQuanta System Spa · 2015
  23. 1 generation backK192539 Deka LuxeaEl.En Electronic Engineering Spa · 2019
  24. This deviceK220794 10PLTentech Co., Ltd. · 2022
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−23K943450Arthrocare Arthroscopic Electrosurgery System Model 970Arthrocare Corp.1995—
−22K961069Arthrocare Urologic Multi-Electrode Electrosurgery SystemArthrocare Corp.1996—
−21K962445Arthrocare Dental Electrosurgery SystemArthrocare Corp.1996—
−20K964849Arthrocare Dermatologic Electrosurgery SystemArthrocare Corp.1997—
−19K973478Arthrocare Sinus Electrosurgery SystemArthrocare Corp.1998—
−18K981870Visage Cosmetic Surgery SystemArthrocare Corp.1998—
−17K000944Thermage Thermacool SystemThermage, Inc.2000—
−16K013034Modification to: Thermacool IiaThermage, Inc.2001—
−15K013639Thermage Thermacool TC SystemThermage, Inc.2002—
−14K021402Thermage Thermacool TC SystemThermage, Inc.2002—
−13K030142Thermacool TC SystemThermage, Inc.2003—
−12K031671Polaris WRSyneron Medical, Ltd.2003—
−11K041959Polaris DS/CometSyneron Medical, Ltd.2004—
−10K053540Intermedic Diode Laser Family 810NM and 980NM (and the Delivery Accessories…Intermedic Arfran, SA2006—
−9K071295100W Ceralas D 980NM Diode LaserBiolitec, Inc.2007—
−8K072106150W Ceralas D 980NM Diode LaserBiolitec, Inc.2007—
−7K083682180W Cerelas D 980NM Diode Laser, Model D180Biolitec, Inc.2009—
−6K082230Vectra Plus Laser System and AccessoriesXintec Corporation2010—
−5K101916Joule Multi-Platform SystemSciton, Inc2011—
−4K140009Soprano Ice Multi-Application & Multi-Technology PlatformAlma Lasers, Ltd.2014—
−3K143519The MeDioStar NeXT FamilyAsclepion Laser Technologies GmbH2015—
−2K152714Quanta ForteQuanta System Spa2015—
−1K192539Deka LuxeaEl.En Electronic Engineering Spa2019—
0 (this device)K22079410PLTentech Co., Ltd.2022—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
197810
198010
198110
198220
198410
198510
198620
198720
198840
198940
199070
1991100
199250
1993120
1994250
1995270
1996300
1997310
1998310
1999270
2000350
2001340
2002450
2003500
2004380
2005320
2006200
2007180
2008210
2009140
201030
201180
201320
201520
201810
FIG. 1 — Lineage of K220794, 1995–2022Source: 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 ONF? 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 ONF device

  1. #1 K233473 Deka Lotusscore 18.2 · 27 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) 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.

TypeNumberDeviceApplicantDecidedRecalls
*K102857Ahwon's Ipl System
Summary page 5
…R 807.92(a)(3)] The identified predicate devices within this submission are shown as follow: Predicate device 1  510(k) Number: K102857  Applicant: Ahwon Medi Instrument.  Classification Name: Laser surgical…
Ahwon Medi Instrument Co., Ltd.2011—
*K181868SHINY RPL System
Summary page 5
…in dermatology  Trade Name: R2PL System Predicate device 2  510(k) Number: K181868  Applicant: IDS, Ltd.  Classification Name: Laser surgical instrument f…
Ids, Ltd.2018—
*K192539Deka Luxea
Summary page 5
…in dermatology  Trade Name: SHINY RPL System Predicate device 3  510(k) Number: K192539  Applicant: El. EN. Electronic Engineering SPA  Classification Name: La…
El.En Electronic Engineering Spa2019—

Also cleared against K102857: 1 other device →

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 27 years and passes through 12 companies; a new generation was cleared every 10 months on median.
  • 28 of the 570 ancestors have a recall of any class.
  • 1 other device also cites its predicate K102857.

How does its category compare?

All ONF devices

ONF Powered Light Based Non-Laser Surgical Instrument With Thermal Effect: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, this device’s year, is highlighted.

FDA decisions per year · ONF

4in 2025

2008: 12009: 52010: 42011: 52012: 32013: 102014: 72015: 32016: 52018: 22019: 22020: 42021: 42022: 42023: 52024: 52025: 42026 (partial year): 1
2007high 10 (2013) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · ONF

192in 2025

2009: 160 days median2010: 137 days median2011: 166 days median2012: 134 days median2013: 113 days median2014: 118 days median2015: 111 days median2016: 87 days median2020: 104 days median2021: 101 days median2022: 165 days median2023: 86 days median2024: 168 days median2025: 192 days median
2007high 192 (2025) · low 86 (2023)2026

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

Recalls per year · ONF

No recall names ONF since 2007.

Adverse event reports per year · ONF

5in 2025

2014: 22015: 42016: 62017: 12018: 12019: 22020: 12021: 22022: 22023: 22024: 32025: 5
2007high 6 (2016) · low 0 (2007)2025

MAUDE reports naming product code ONF, 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
20070—00
20081—00
2009516000
2010413700
2011516600
2012313400
20131011300
2014711802
2015311104
201658706
20170—01
20182—01
20192—02
2020410401
2021410102
2022416502
202358602
2024516803
2025419205
20261—0—

What is it indicated for?

The Photo therapy unit (model: 10PL) is intended for use in surgical and aesthetic applications in dermatology by using filtered Intense Pulsed Light to treat the following conditions with different wavelengths to skin types I-IV.

Wavelengths Conditions

415nm - 950nm Melasma

570nm - 950nm Melasma, Rosacea

590nm - 950nm Rosacea, Port wine stains

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. “K220794: 10PL.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K220794

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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