510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K230459Substantially Equivalent

C.C. Life 21

21 Equipment S.r.l., Torino, IT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K230459 is the FDA 510(k) clearance record for C.C. Life 21, a class II device, cleared for 21 Equipment S.R.L. on under FDA product code NFO (Stimulator, Transcutaneous Electrical, Aesthetic Purposes). FDA records list 2 510(k) clearances for 21 Equipment S.R.L., from to . As of , FDA records show no recalls naming K230459.

Clearance record

Decision date
Received
(240 days to decision)
Product code
NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes
Regulation
21 CFR 882.5890
Device class
Class II
Review panel
Neurology
Applicant
21 Equipment S.R.L. Piazza Bodoni 3, Torino, IT
510(k) summary
Statement
Third party review
No

Clearances, product code NFO

Trailing 12 months
9 clearances under product code NFO in the twelve months to October 2026, December 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code NFO, trailing twelve months
MonthClearances
November 20250
December 20252
January 20260
February 20260
March 20260
April 20260
May 20262
June 20261
July 20261
August 20261
September 20262
October 20260