Varpr 3.5mm 90 Suction Electrode for Use with Vapr System

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K002422 ↗

FDA Product Code

GEI

Device Class

Class II

Regulation

21 CFR Part 878.4400

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Mitek Absorbable Toggle Anchor

  Class II

  FDA 510(k) K964013 Active Cleared 24 Feb 1997

• Resolve Quickanchor

  Class II

  FDA 510(k) K993575 Active Cleared 29 Dec 1999

• Mitek Knotless Anchor

  Class II

  FDA 510(k) K974345 Active Cleared 13 Feb 1998

• Mitek Btb Absorbable (Pla) Cross Pin

  Class II

  FDA 510(k) K974341 Active Cleared 16 Apr 1998

• Rididfix 2.7mm Btb Cross Pin Kit

  Class II

  FDA 510(k) K013781 Active Cleared 6 Feb 2002

• BioKnotless Anchor

  Class II

  FDA 510(k) K002639 Active Cleared 11 May 2001

See all devices from Mitek Products →