Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K961076Substantially Equivalent

Mm 324

Micro-Mega Societe Anonyme, Besancon, FR / Traditional, Substantially Equivalent

K961076 is the FDA 510(k) clearance record for MM 324, a class I device, cleared for Micro-Mega Societe Anonyme on under FDA product code EFB (Handpiece, Air-Powered, Dental). FDA records list 11 510(k) clearances for Micro-Mega Societe Anonyme, from to . As of , FDA records show no recalls naming K961076.

Clearance record

Decision date
Received
(39 days to decision)
Product code
EFB Handpiece, Air-Powered, Dental
Regulation
21 CFR 872.4200
Device class
Class I
Review panel
Dental
Applicant
Micro-Mega Societe Anonyme 5-12 Rue Du Tunnel, Besancon, FR
510(k) summary
Statement
Third party review
No

Clearances, product code EFB

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