510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K231023Substantially Equivalent

ERBEJET® 2 System

ERBE Elektromedizin GmbH, Tuebingen, DE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K231023 is the FDA 510(k) clearance record for ERBEJET® 2 System, a class II device, cleared for Erbe Elektromedizin GmbH on under FDA product code FQH (Lavage, Jet). FDA records list 16 510(k) clearances for Erbe Elektromedizin GmbH, from to . As of , FDA records show no recalls naming K231023.

Clearance record

Decision date
Received
(65 days to decision)
Product code
FQH Lavage, Jet
Regulation
21 CFR 880.5475
Device class
Class II
Review panel
General Hospital
Applicant
Erbe Elektromedizin GmbH Waldhoernlestrasse 17, Tuebingen, DE
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FQH

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