510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K142995Substantially Equivalent

Sopix

Sopro - Acteon Group, Laciotat, FR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K142995 is the FDA 510(k) clearance record for SOPIX, a class II device, cleared for Sopro - Acteon Group on under FDA product code MUH (System, X-Ray, Extraoral Source, Digital). FDA records list 4 510(k) clearances for Sopro - Acteon Group, from to . As of , FDA records show no recalls naming K142995.

Clearance record

Decision date
Received
(305 days to decision)
Product code
MUH System, X-Ray, Extraoral Source, Digital
Regulation
21 CFR 872.1800
Device class
Class II
Review panel
Dental
Applicant
Sopro - Acteon Group
510(k) summary
Statement
Third party review
No

Clearances, product code MUH

Trailing 12 months
2 clearances under product code MUH in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code MUH, trailing twelve months
MonthClearances
November 20251
December 20250
January 20260
February 20260
March 20261
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260