Neuro & Craniofacial Fixation System

FDA UDI

Class I (US FDA UDI)

by Innovasis, Inc.

Identity

Trade Name: Neuro & Craniofacial Fixation System FDA UDI
Generic Name: Implant handling forceps, tweezers-like FDA UDI
Device Name: SST FDA UDI
Model / Reference: LS-422 FDA UDI
Description: SST FDA UDI

Identifiers

Catalog Number: LS-422 FDA UDI
Primary DI / UDI-DI: M711LS4220 FDA UDI
FDA Product Code: HTD FDA UDI
GMDN Term: Implant handling forceps, tweezers-like FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Implant handling forceps, tweezers-like

Neuro & Craniofacial Fixation System by Innovasis, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Implant handling forceps, tweezers-like.

Comfort Drain Grasper — AMI Agency for Medical Innovations GmbH · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Innovasis, Inc.

Sources (1)

FDA UDI 2f3dddee-c5b1-4f87-b5b0-591460976f44 35 fields · synced Jun 1, 2026