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Combined Submalar Shell™

FDA UDI

Class II (US FDA UDI)

by Implantech Associates, Inc.

Identity

Trade Name
Combined Submalar Shell™ FDA UDI
Generic Name
Malar prosthesis FDA UDI
Device Name
Midfacial Implant FDA UDI
Model / Reference
Size: Small FDA UDI
Description
Midfacial Implant FDA UDI

Identifiers

Catalog Number
CSM-S-NS FDA UDI
Primary DI / UDI-DI
M724CSMSNS1 FDA UDI
510(k) Number
K910655 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

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Malar prosthesis

Combined Submalar Shell™ by Implantech Associates, Inc. — 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

Sources (1)

  • FDA UDI a6b0c368-4ddd-4493-be7a-32a2c4200d6f 36 fields · synced Jun 9, 2026