510(k) Report

510(k) · Cleared

Cleared

Electronic Depilatory Model 303

K770187510(k) TraditionalCleared Feb 23, 197727-day reviewClass I21 CFR 878.5360

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

Electronic Depilatory, Inc. · KCX Epilator, High Frequency, Tweezer-Type

Cleared on Feb 23, 1977 after a 27-day review. FDA has not posted a summary or statement for it, so its predicates are not known.

Decided
Feb 23, 1977
Review
27 days
Class
Class I
Product code
KCX
Recalls
None
Predicates
0

FDA has not posted a summary or statement for it, so its predicates are not known.

FIG. 1 — Lineage of K770187Source: FDA 510(k) database · How lineage is built

Get the monthly Device Review Tracker

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

Sources: FDA 510(k) database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in KCX? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

  • Candidate predicates for a device like this, rankedin the report
  • Recall history across each candidate’s familyin the report
Get a 510(k) Report

What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

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.

How does its category compare?

All KCX devices

KCX Epilator, High Frequency, Tweezer-Type: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · KCX

FDA has decided no KCX device since 2007.

Median 510(k) review, days · KCX

Too few KCX 510(k)s in any year since 2007 to give a median.

Recalls per year · KCX

No recall names KCX since 2007.

Adverse event reports per year · KCX

1in 2014

2012: 22014: 1
2007high 2 (2012) · low 0 (2007)2025

MAUDE reports naming product code KCX, 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
20080—00
20090—00
20100—00
20110—00
20120—02
20130—00
20140—01
20150—00
20160—00
20170—00
20180—00
20190—00
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—

More from Electronic Depilatory, Inc.

3 FDA decisions under this applicant name. See the company

  • K771575Electronic Eiplator Model NO. 101Electronic Depilatory, Inc. · 1977
  • K770186Electronic Depilatory Model 202Electronic Depilatory, Inc. · 1977

Recent decisions in KCX

The KCX category page

  • K973773Dapelle Hair RemoverWellquest Intl., Inc. · 1997
  • K973340Tweezer-Type EpilatorMobit, Inc. · 1997
  • K973179Feminique Sonic Hair RemoverGlobal TV Concepts, Ltd. · 1997
  • K973174Sonique Hair RemoverGlobal TV Concepts, Ltd. · 1997
  • K972695Finally FreeMehl/Group Marketing · 1997

https://510kreport.com/device/K770187 · printed Nov 6, 2026

Cite this page

510(k) Report. “K770187: Electronic Depilatory Model 303.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K770187

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

Record history
  • FDA decision record loaded May 2, 2026
  • Page last updated Nov 3, 2026