Scalpel Remover

FDA UDI

Class I (US FDA UDI)

by Suncoast Dental, Inc.

Identity

Trade Name: Scalpel Remover FDA UDI
Generic Name: Dental prosthesis removal instrument FDA UDI
Device Name: Scalpel Removers, Curved Tip, Tungsten Carbide Tip. To grip and remove Scalpel blades safely from patient and or from scalpel handles. FDA UDI
Model / Reference: Scalpel Remover T/C FDA UDI
Description: Scalpel Removers, Curved Tip, Tungsten Carbide Tip. To grip and remove Scalpel blades safely from patient and or from scalpel handles. FDA UDI

Identifiers

Catalog Number: Scalpel Remover T/C FDA UDI
Primary DI / UDI-DI: 00083208130519 FDA UDI
FDA Product Code: DZN FDA UDI
GMDN Term: Dental prosthesis removal instrument FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.4565 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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Dental prosthesis removal instrument

Scalpel Remover by Suncoast Dental, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Dental prosthesis removal instrument.

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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: Suncoast Dental, Inc.

Sources (1)

FDA UDI 0a743bd6-d3f4-4d03-8532-5caf207c61a9 35 fields · synced May 30, 2026