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Ilizarov

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
ILIZAROV FDA UDI
Generic Name
Surgical torque wrench, reusable FDA UDI
Device Name
WRENCH 10MM AND 13MM FDA UDI
Model / Reference
L202002 FDA UDI
Description
WRENCH 10MM AND 13MM FDA UDI

Identifiers

Catalog Number
L202002 FDA UDI
Primary DI / UDI-DI
03596010432346 FDA UDI
510(k) Number
K093047 FDA UDI
FDA Product Code
KTT FDA UDI
GMDN Term
Surgical torque wrench, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 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: Surgical torque wrench, reusable

Ilizarov by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical torque wrench, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4c3636aa-13b3-4058-8c9e-ce55840e7368 36 fields · synced Jun 8, 2026