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Reflection, Microstable

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
REFLECTION, MICROSTABLE FDA UDI
Generic Name
Acetabulum prosthesis trial, prefabricated, reusable FDA UDI
Device Name
REF LNR 22ID 40 OD 20 DEG FDA UDI
Model / Reference
71742240 FDA UDI
Description
REF LNR 22ID 40 OD 20 DEG FDA UDI

Identifiers

Catalog Number
71742240 FDA UDI
Primary DI / UDI-DI
03596010000644 FDA UDI
510(k) Number
K920430 FDA UDI
FDA Product Code
JDI FDA UDI
GMDN Term
Acetabulum prosthesis trial, prefabricated, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3350 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Acetabulum prosthesis trial, prefabricated, reusable

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

Similar devices

Also classified as Acetabulum prosthesis trial, prefabricated, reusable.

Cleared under the same submission

K920430 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4c6d93e8-ccbb-4fc5-a21b-cd0a754d5724 36 fields · synced Jun 8, 2026