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Fallopian Tube Forceps

by American V. Mueller

510(k) K810483

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 6 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 6 Oct 2026. What this means

Regulatory status

as of registry sync 6 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK810483 Date11 Mar 1981ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 6 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
KNA
Device Class
Class II
Regulation
21 CFR Part 884.4530
Advisory Committee
Obstetrics/Gynecology
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 19 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

The Fallopian Tube Forceps is a Manual, Specialized Obstetric-Gynecologic Instrument designed for precise grasping and manipulation of fallopian tube tissue during surgical procedures. Classified as a Class II device, it is intended for use in minimally invasive and open gynecological surgeries, including tubal ligation or other fallopian tube interventions.

Supplied as a reusable surgical tool, the device is intended for single-patient use per sterile packaging. Models such as the LA1354F feature a 5mm x 33cm shaft with a ratchet mechanism and flush port, with an overall length of 8-1/8

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Questions

AI-generated answers, 19 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

  • What surgical procedures is this Fallopian Tube Forceps designed to assist with, and how does it differ from standard forceps?

    The Fallopian Tube Forceps is specifically designed for precise grasping and manipulation of fallopian tube tissue during gynecological surgeries, such as tubal ligation or other fallopian tube interventions. Unlike standard forceps, it features specialized design elements like a ratchet mechanism and a flush port, which enhance control and stability when working with delicate fallopian tube tissue. It is intended for use in both minimally invasive and open surgical procedures.

  • Is this device reusable or single-use, and how is it packaged for sterility?

    The Fallopian Tube Forceps is a reusable surgical tool, but it is supplied in sterile packaging intended for single-patient use. This ensures that each patient receives a clean and sterile instrument, reducing the risk of infection while allowing for proper reprocessing between uses in a clinical setting.

  • What are the key dimensions and features of the LA1354F model, and how does the shaft length compare to other models?

    The LA1354F model features a shaft measuring 5mm in width by 33cm in length, with an overall length of 8-1/8 inches. This design provides a balance of precision and reach for delicate fallopian tube procedures. While the exact dimensions of other models aren’t specified, the shaft length and width are tailored to facilitate controlled manipulation during gynecological surgeries.

  • How should this device be stored to maintain its integrity and sterility?

    Since the Fallopian Tube Forceps is reusable and supplied in sterile packaging for single-patient use, it should be stored in a clean, dry environment away from direct sunlight or extreme temperatures. After use, it must undergo proper reprocessing (cleaning, disinfection, and sterilization) before storage to ensure sterility for subsequent procedures. Always follow manufacturer guidelines for storage and reprocessing.