510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K896749Substantially Equivalent

Piezon Master 400

E.M.S. - Electro Medical Systems SA, Nyon, CH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K896749 is the FDA 510(k) clearance record for PIEZON MASTER 400, a class II device, cleared for Electro Medical Systems (Ems Sa) on under FDA product code ELC (Scaler, Ultrasonic). FDA records list 41 510(k) clearances for E.M.S. ELECTRO MEDICAL SYSTEMS S.A., from to . As of , FDA records show no recalls naming K896749.

Clearance record

Decision date
Received
(274 days to decision)
Product code
ELC Scaler, Ultrasonic
Regulation
21 CFR 872.4850
Device class
Class II
Review panel
Dental
Applicant
Electro Medical Systems (Ems Sa) Ch. De La Vuarpilliere 31, Nyon, CH
Third party review
No

Clearances, product code ELC

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