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ALPHALOK Plating System

FDA UDI

Class I (US FDA UDI)

by Vilex, Inc.

Identity

Trade Name
ALPHALOK Plating System FDA UDI
Generic Name
Self-retaining surgical retractor, reusable FDA UDI
Device Name
Distractor 6", Max Cap. 2.4mm FDA UDI
Model / Reference
TL-DIST FDA UDI
Description
Distractor 6", Max Cap. 2.4mm FDA UDI

Identifiers

Catalog Number
TL-DIST FDA UDI
Primary DI / UDI-DI
00841731129789 FDA UDI
FDA Product Code
GAD FDA UDI
GMDN Term
Self-retaining surgical retractor, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Self-retaining surgical retractor, reusable

ALPHALOK Plating System by Vilex, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Self-retaining surgical retractor, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vilex, Inc.

Sources (1)

  • FDA UDI fc82386e-ae7b-4383-8e2a-7deec5156ce4 34 fields · synced May 30, 2026