Microsurge Front-End Grasping Devices

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

510(k) Number

K922802 ↗

FDA Product Code

GEI

Device Class

Class II

Regulation

21 CFR Part 878.4400

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Microsurge Thoracoscopic Instruments

  Class II

  FDA 510(k) K955408 Active Cleared 31 Jan 1996

• Microsurge Detacha-Tip Surgical Instruments

  Class II

  FDA 510(k) K924283 Active Cleared 7 Apr 1993

• Microsurge Laser Fiber with Sma Connector

  Class II

  FDA 510(k) K914175 Active Cleared 17 Dec 1991

• Microsurge Laser Fiber Holder

  Class II

  FDA 510(k) K912332 Active Cleared 21 Aug 1991

• Detachatip Thoracoscopic Scissors

  Class II

  FDA 510(k) K960554 Active Cleared 5 Mar 1996

• Microsurge Bipolar Graspers

  Class II

  FDA 510(k) K951230 Active Cleared 14 Jun 1995

See all devices from Microsurge, Inc. →

• What are Microsurge Front-End Grasping Devices used for?

  These instruments are specifically designed to grasp and manipulate anatomical structures within the surgical field. They are intended for use by clinicians performing general and plastic surgery procedures.

• What is the regulatory status of this device?

  The Microsurge Front-End Grasping Devices have received FDA 510(k) clearance under the submission number K922802. This indicates the device has been determined to be substantially equivalent to legally marketed predicate devices.

• Who is the manufacturer of these grasping devices?

  The devices are manufactured by Microsurge, Inc., located in North Attleboro, Massachusetts. The company submitted the device for regulatory review, which resulted in a decision of substantial equivalence in January 1993.