Worldwide Medical Technologies Seeding Spacers

No FDA recalls found in the data synced 10 Oct 2026.

510(k) Number

K991344 ↗

FDA Product Code

KXK

Device Class

Class II

Regulation

21 CFR Part 892.5730

Advisory Committee

Radiology

FDA Decision

SESE Substantially Equivalent

• Worldwide Medical Technologies Needle Guide

  Class II

  FDA 510(k) K981470 Active Cleared 19 Jun 1998

• Readi-Load System, Model Pss 1820RL

  Class II

  FDA 510(k) K022389 Active Cleared 6 May 2003

• Worldwide Medical Technologies I Type Needle

  Class II

  FDA 510(k) K980068 Active Cleared 23 Jan 1998

• Readi-Strand, Model Psstrand

  Class II

  FDA 510(k) K022705 Active Cleared 9 Jun 2003

• Worldwide Medical Technologies Intracervical Block Needle, Model Tbd

  Class II

  FDA 510(k) K982097 Active Cleared 25 Jun 1998

• Worldwide Medical Technologies Seed Implant Needle Set

  Class I

  FDA 510(k) K974118 Active Cleared 23 Jan 1998

See all devices from Worldwide Medical Technologies, LLC →