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Reflection

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
REFLECTION FDA UDI
Generic Name
Ceramic acetabular liner FDA UDI
Device Name
REFLECTION ACETABULAR LINER 32MM INNER DIAMETER X 62-64MM W/35 DEGREE LIP FDA UDI
Model / Reference
71923738 FDA UDI
Description
REFLECTION ACETABULAR LINER 32MM INNER DIAMETER X 62-64MM W/35 DEGREE LIP FDA UDI

Identifiers

Catalog Number
71923738 FDA UDI
Primary DI / UDI-DI
03596010427953 FDA UDI
510(k) Number
K932755 FDA UDI
FDA Product Code
LPH FDA UDI
GMDN Term
Ceramic acetabular liner FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3358 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ceramic acetabular liner

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

Similar devices

Also classified as Ceramic acetabular liner.

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 c0eaca23-95d1-4ed6-8e45-ad22a7819cc0 36 fields · synced Jun 8, 2026