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Conquest Fn

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
CONQUEST FN FDA UDI
Generic Name
Surgical depth gauge, reusable FDA UDI
Device Name
CONQUEST FN PROXIMAL SCREW DEPTH GAUGE FDA UDI
Model / Reference
71179207 FDA UDI
Description
CONQUEST FN PROXIMAL SCREW DEPTH GAUGE FDA UDI

Identifiers

Catalog Number
71179207 FDA UDI
Primary DI / UDI-DI
00885556533123 FDA UDI
510(k) Number
K152686 FDA UDI
FDA Product Code
KTT FDA UDI
JDO FDA UDI
GMDN Term
Surgical depth gauge, 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

No

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 depth gauge, reusable

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

Similar devices

Also classified as Surgical depth gauge, 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 3e3578ff-2efc-494f-9b97-9fd3da785c26 36 fields · synced Jun 8, 2026