Reflection

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name: REFLECTION FDA UDI
Generic Name: Acetabular shell FDA UDI
Device Name: REFLECTION TRIAL ACETABULAR SHELL 59MM OD FDA UDI
Model / Reference: 730059 FDA UDI
Description: REFLECTION TRIAL ACETABULAR SHELL 59MM OD FDA UDI

Identifiers

Catalog Number: 730059 FDA UDI
Primary DI / UDI-DI: 03596010258243 FDA UDI
510(k) Number: K123598 FDA UDI
FDA Product Code: JDG FDA UDI
GMDN Term: Acetabular shell FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3360 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

Yes

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

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: Acetabular shell

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

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Cleared under the same submission

K123598 also covers:

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 II	Pending data

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Manufacturer

Manufacturer: Smith & Nephew, Inc.

Sources (1)

FDA UDI 5b2395fb-eaba-4ec2-bc9d-8c51fe47da3d 36 fields · synced Jun 8, 2026