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Spectrum Designs Medical

FDA UDI

Class II (US FDA UDI)

by Spectrum Designs, Inc.

Identity

Trade Name
Spectrum Designs Medical FDA UDI
Generic Name
Malar prosthesis FDA UDI
Device Name
Allergan Distributed FDA UDI
Model / Reference
Extended Malar, size 3 FDA UDI
Description
Allergan Distributed FDA UDI

Identifiers

Catalog Number
150-534S FDA UDI
Primary DI / UDI-DI
B018150534S1 FDA UDI
FDA Product Code
LZK FDA UDI
GMDN Term
Malar prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.3550 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Malar prosthesis

Spectrum Designs Medical by Spectrum Designs, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Malar prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6a5410d3-c5b0-49f5-a596-82216cdeb6e2 35 fields · synced May 30, 2026