Whistler Modular Pedicle Screw System

FDA UDI

Class I (US FDA UDI)

by Evolution Spine, Llc

Identity

Trade Name: Whistler Modular Pedicle Screw System FDA UDI
Generic Name: Surgical screwdriver, reusable FDA UDI
Device Name: Axial Persuader Final Tightening Driver FDA UDI
Model / Reference: WI-059 FDA UDI
Description: Axial Persuader Final Tightening Driver FDA UDI

Identifiers

Catalog Number: WI-059 FDA UDI
Primary DI / UDI-DI: 00195860005132 FDA UDI
FDA Product Code: LXH FDA UDI
GMDN Term: Surgical screwdriver, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.4540 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Surgical screwdriver, reusable

Whistler Modular Pedicle Screw System by Evolution Spine, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Surgical screwdriver, reusable.

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PERLA ® TL — Spineart · Class II
USS — Synthes · Class I
CosmoLock Pedicle Screw System — Kalitec Direct LLC · Class I
KLOCKNER — SOADCO, S.L. · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Evolution Spine, Llc

Sources (1)

FDA UDI f7aaa0f6-f2ae-4bdb-bfa5-bf9365a2a132 35 fields · synced May 30, 2026