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Clarity® Lateral Retractor System 38-Thinblade-100

by Pioneer Surgical Technology, Inc.

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Overview

The Clarity Lateral Retractor System is a thin blade orthopedic manual surgical instrument designed for the placement of internal orthopaedic fixation systems into various bones, including limbs, spine, pelvis, and craniomaxillofacial bones. This reusable device features a general internal orthopaedic fixation system implantation kit design and has been used in orthopedic surgeries for over 8 years.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00846468011796 UDI-DI Date16 Jun 2016ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Clarity® Lateral Retractor System
Generic Name
General internal orthopaedic fixation system implantation kit
Model / Reference
38-THINBLADE-100
Primary DI / UDI-DI
00846468011796
FDA Product Code
LXH
GMDN Term
General internal orthopaedic fixation system implantation kit
Device Class
Class I
Regulation Number
888.4540
GUDID distribution status
Not in Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

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Properties

  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No