510(k) Report

510(k) · Cleared

Cleared

Newa Skin Therapy System

K130793510(k) TraditionalCleared Aug 16, 2013147-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

Endymion Medical, Ltd. · GEI Electrosurgical, Cutting & Coagulation & Accessories

Cleared on Aug 16, 2013 as substantially equivalent to K083461 (Endymion Medical, Ltd., 2009) and 1 other predicate after a 147-day review. Its family tree reaches back 15 generations to 1995.

Decided
Aug 16, 2013
Review
147 days
Class
Class II
Product code
GEI
Recalls
None
Predicates
2

Its longest line of descent runs back 15 generations to K943450 (1995). 199 ancestors in all, the oldest K800617 (1980). No later device cites it as a predicate yet.

Other ancestors, by year cleared 2009: 1 other ancestor2008: 2 other ancestors2007: 2 other ancestors2005: 4 other ancestors2006: 1 other ancestor2004: 5 other ancestors2003: 14 other ancestors2002: 18 other ancestors2001: 12 other ancestors2000: 17 other ancestors1999: 9 other ancestors1998: 14 other ancestors1997: 19 other ancestors1996: 19 other ancestors1995: 12 other ancestors1994: 14 other ancestors1990: 2 other ancestors1988: 1 other ancestor1982: 2 other ancestors1991: 5 other ancestors1986: 1 other ancestor1993: 5 other ancestors1992: 3 other ancestors1980: 1 other ancestor1985: 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. · 2003K051214 · Aluma Skin Renewal System · Lumenis, Inc. · 2005K070004 · Accent · Alma Lasers, Ltd. · 2007K083461 · Imagine TC Skin Therapy System · Endymion Medical, Ltd. · 200919801985199019952000200520102015
Other ancestors, by generation 1 generation back: 1 other ancestor2 generations back: 4 other ancestors3 generations back: 12 other ancestors4 generations back: 48 other ancestors5 generations back: 36 other ancestors6 generations back: 44 other ancestors7 generations back: 25 other ancestors8 generations back: 11 other ancestors9 generations back: 2 other ancestors10 generations back: 1 other ancestor K083461 · Imagine TC Skin Therapy System · Endymion Medical, Ltd. · 2009K070004 · Accent · Alma Lasers, Ltd. · 2007K051214 · Aluma Skin Renewal System · Lumenis, Inc. · 2005K031671 · 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. · 1995−15−10−50
  1. Root · 15 generations backK943450 Arthrocare Arthroscopic Electrosurgery System Model 970Arthrocare Corp. · 1995
  2. 11 generations between
  3. 3 generations backK051214 Aluma Skin Renewal SystemLumenis, Inc. · 2005
  4. 2 generations backK070004 AccentAlma Lasers, Ltd. · 2007
  5. 1 generation backK083461 Imagine TC Skin Therapy SystemEndymion Medical, Ltd. · 2009
  6. This deviceK130793 Newa Skin Therapy SystemEndymion Medical, Ltd. · 2013
Show all 15 generations
  1. Root · 15 generations backK943450 Arthrocare Arthroscopic Electrosurgery System Model 970Arthrocare Corp. · 1995
  2. 14 generations backK961069 Arthrocare Urologic Multi-Electrode Electrosurgery SystemArthrocare Corp. · 1996
  3. 13 generations backK962445 Arthrocare Dental Electrosurgery SystemArthrocare Corp. · 1996
  4. 12 generations backK964849 Arthrocare Dermatologic Electrosurgery SystemArthrocare Corp. · 1997
  5. 11 generations backK973478 Arthrocare Sinus Electrosurgery SystemArthrocare Corp. · 1998
  6. 10 generations backK981870 Visage Cosmetic Surgery SystemArthrocare Corp. · 1998
  7. 9 generations backK000944 Thermage Thermacool SystemThermage, Inc. · 2000
  8. 8 generations backK013034 Modification to: Thermacool IiaThermage, Inc. · 2001
  9. 7 generations backK013639 Thermage Thermacool TC SystemThermage, Inc. · 2002
  10. 6 generations backK021402 Thermage Thermacool TC SystemThermage, Inc. · 2002
  11. 5 generations backK030142 Thermacool TC SystemThermage, Inc. · 2003
  12. 4 generations backK031671 Polaris WRSyneron Medical, Ltd. · 2003
  13. 3 generations backK051214 Aluma Skin Renewal SystemLumenis, Inc. · 2005
  14. 2 generations backK070004 AccentAlma Lasers, Ltd. · 2007
  15. 1 generation backK083461 Imagine TC Skin Therapy SystemEndymion Medical, Ltd. · 2009
  16. This deviceK130793 Newa Skin Therapy SystemEndymion Medical, Ltd. · 2013
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−15K943450Arthrocare Arthroscopic Electrosurgery System Model 970Arthrocare Corp.1995—
−14K961069Arthrocare Urologic Multi-Electrode Electrosurgery SystemArthrocare Corp.1996—
−13K962445Arthrocare Dental Electrosurgery SystemArthrocare Corp.1996—
−12K964849Arthrocare Dermatologic Electrosurgery SystemArthrocare Corp.1997—
−11K973478Arthrocare Sinus Electrosurgery SystemArthrocare Corp.1998—
−10K981870Visage Cosmetic Surgery SystemArthrocare Corp.1998—
−9K000944Thermage Thermacool SystemThermage, Inc.2000—
−8K013034Modification to: Thermacool IiaThermage, Inc.2001—
−7K013639Thermage Thermacool TC SystemThermage, Inc.2002—
−6K021402Thermage Thermacool TC SystemThermage, Inc.2002—
−5K030142Thermacool TC SystemThermage, Inc.2003—
−4K031671Polaris WRSyneron Medical, Ltd.2003—
−3K051214Aluma Skin Renewal SystemLumenis, Inc.2005—
−2K070004AccentAlma Lasers, Ltd.2007—
−1K083461Imagine TC Skin Therapy SystemEndymion Medical, Ltd.2009—
0 (this device)K130793Newa Skin Therapy SystemEndymion Medical, Ltd.2013—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198010
198220
198510
198610
198810
199020
199150
199230
199350
1994140
1995120
1996190
1997190
1998140
199990
2000170
2001120
2002180
2003140
200450
200540
200610
200720
200820
200910
FIG. 1 — Lineage of K130793, 1995–2013Source: 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
Get a 510(k) 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.

TypeNumberDeviceApplicantDecidedRecalls
*K083461Imagine TC Skin Therapy System
Summary page 1
…Date of Clearance Imagine TC Skin Treatment System EndyMed Medical K083461 Jul124, 2009 Ltd. (previously…
Endymion Medical, Ltd.2009—
*K090525Loi System
Summary page 1
…Ltd. (previously EndyMion Medical) Palomar LOI System Palomar Medical K090525 June 1, 2009 ___________________________ Technologies, Inc. _ _ _ _ ________ === Page 2 ==…
Palomar Medical Products, Inc.2009—

Also cleared against K083461: 11 other devices →

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 18 years and passes through 6 companies; a new generation was cleared every 10 months on median.
  • 7 of the 199 ancestors have a recall of any class.
  • 11 other devices also cite its predicate K083461.

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. 2013, 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 EndyMed Newa™ is a prescription home use device intended for non-invasive treatment of mild to moderate facial wrinkles and rhytides

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K130793: Newa Skin Therapy System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K130793

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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