510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K954722Substantially Equivalent

Micro-Dispenser 7000 & Microdispenser 8000

Nouvag AG, Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K954722 is the FDA 510(k) clearance record for MICRO-DISPENSER 7000 & MICRODISPENSER 8000, a class I device, cleared for NOUVAG AG on under FDA product code EFB (Handpiece, Air-Powered, Dental). FDA records list 11 510(k) clearances for NOUVAG AG, from to . As of , FDA records show no recalls naming K954722.

Clearance record

Decision date
Received
(95 days to decision)
Product code
EFB Handpiece, Air-Powered, Dental
Regulation
21 CFR 872.4200
Device class
Class I
Review panel
Dental
Applicant
Nouvag Ag 555 Thirteen St., NW, Washington DC
510(k) summary
Summary
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