Erbe Vio Esu with Accessories, Model Vio 300 D

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K023886 ↗

FDA Product Code

GEI

Device Class

Class II

Regulation

21 CFR Part 878.4400

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Erbe Model Vio 300 D with Accessories

  Class II

  FDA 510(k) K083452 Active Cleared 31 Dec 2008

• Erbotom Icc 50

  Class II

  FDA 510(k) K935815 Active Cleared 31 Mar 1994

• Erbe's Tubing/Cap Sets Open recall

  Class II

  FDA 510(k) K221177 Active Cleared 11 Aug 2022

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  Class II

  FDA 510(k) K151041 Active Cleared 4 May 2015

• Erbeflo 2 Disposable Tubing System

  Class II

  FDA 510(k) K103235 Active Cleared 23 Dec 2010

• Erbe Esu Model Vio 100 C with Accessories

  Class II

  FDA 510(k) K101108 Active Cleared 16 Jul 2010

See all devices from Erbe USA, Inc. →