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Malar Implant

FDA UDI

Class II (US FDA UDI)

by Aart

Identity

Trade Name
Malar Implant FDA UDI
Generic Name
Malar prosthesis FDA UDI
Device Name
Malar Style 1 Size 3 Left FDA UDI
Model / Reference
D FDA UDI
Description
Malar Style 1 Size 3 Left FDA UDI

Identifiers

Catalog Number
401-103-5 FDA UDI
Primary DI / UDI-DI
B4904011035 FDA UDI
510(k) Number
K021419 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

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI
Sterilization Method
Dry Heat Sterilization FDA UDI

Category: Malar prosthesis

Malar Implant by Aart — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Malar prosthesis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aart

Sources (1)

  • FDA UDI 473f9736-c195-4e0f-9b35-561c1324f696 36 fields · synced Jun 6, 2026