510(k) Report

510(k) · Cleared

Cleared

Tua Face Fitness / Tua Trend Face

K192077510(k) TraditionalCleared Sep 30, 2020425-day reviewClass II21 CFR 882.5890

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

Vupiesse S.R.L · NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes

Cleared on Sep 30, 2020 as substantially equivalent to K103031 (Bio-Medical Research, Ltd., 2011) after a 425-day review. Its family tree reaches back 2 generations to 2001.

Decided
Sep 30, 2020
Review
425 days
Class
Class II
Product code
NFO
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K011935 (2001). No later device cites it as a predicate yet.

  1. Root · 2 generations backK011935 Rejuvenique Model #RJV10Salton, Inc. · 2001
  2. 1 generation backK103031 BMR FaceBio-Medical Research, Ltd. · 2011
  3. This deviceK192077 Tua Face Fitness / Tua Trend FaceVupiesse S.R.L · 2020
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K011935Rejuvenique Model #RJV10Salton, Inc.2001—
−1K103031BMR FaceBio-Medical Research, Ltd.2011—
0 (this device)K192077Tua Face Fitness / Tua Trend FaceVupiesse S.R.L2020—
FIG. 1 — Lineage of K192077, 2001–2020Source: 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 NFO? 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 NFO device

  1. #1 K233010 Beagank 4T Plusscore 28.6 · 5 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
*K103031BMR Face
Summary page 4
…Product Code: NFO Device Class: 2 4. Identification of Equivalent Legally Marketed Device 510(k) Number: K103031 Clearance Date: 11/10/2011 Regulation Number: 21CFR 882.5890 Manufacturer: B…
Bio-Medical Research, Ltd.2011—

Also cleared against K103031: 2 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 19 years and passes through 3 companies; a new generation was cleared every 10.3 years on median.
  • None of the 2 ancestors has a recall.
  • 2 other devices also cite its predicate K103031.

How does its category compare?

All NFO devices

NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.

FDA decisions per year · NFO

16in 2025

2007: 12008: 32011: 32012: 32013: 22014: 22015: 22016: 22017: 72018: 52019: 32020: 22021: 72022: 22023: 82024: 52025: 162026 (partial year): 8
2007high 16 (2025) · low 0 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NFO

124in 2025

2008: 550 days median2011: 394 days median2012: 160 days median2017: 189 days median2018: 177 days median2019: 149 days median2021: 210 days median2023: 128 days median2024: 109 days median2025: 124 days median2026 (partial year): 153 days median
2007high 550 (2008) · low 109 (2024)2026

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

Recalls per year · NFO

2in 2012

2012: 2
2007high 2 (2012) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · NFO

4in 2025

2011: 12013: 12015: 12016: 52019: 12020: 62021: 62022: 52023: 12024: 42025: 4
2007high 6 (2020) · low 0 (2007)2025

MAUDE reports naming product code NFO, 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
20071—00
2008355000
20090—00
20100—00
2011339401
2012316020
20132—01
20142—00
20152—01
20162—05
2017718900
2018517700
2019314901
20202—06
2021721006
20222—05
2023812801
2024510904
20251612404
202681530—

What is it indicated for?

Tua Face Fitness / Tua Trend Face is a device intended for facial stimulation and is indicated for Over-the-Counter cosmetic use.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K192077: Tua Face Fitness / Tua Trend Face.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K192077

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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