← Back to catalogue

Surgiform

FDA UDI

Class II (US FDA UDI)

by Surgical Technology Laboratories Inc.

Identity

Trade Name
Surgiform FDA UDI
Generic Name
Malar prosthesis FDA UDI
Device Name
"ETM-04 Extended Trapezoidal Malar Silicone Implants" FDA UDI
Model / Reference
ETM-04 FDA UDI
Description
"ETM-04 Extended Trapezoidal Malar Silicone Implants" FDA UDI

Identifiers

Catalog Number
ETM-04 FDA UDI
Primary DI / UDI-DI
00851988007365 FDA UDI
510(k) Number
K983756 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

Surgiform by Surgical Technology Laboratories 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 9a239eb5-32af-42af-9bc3-94b561dc8192 35 fields · synced May 30, 2026