Curad

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name: Curad FDA UDI
Generic Name: Orthodontic appliance remover FDA UDI
Device Name: CURAD,PROSORB,ROLLGAUZE,3"X 90", 5CT FDA UDI
Model / Reference: CUR4731435RB FDA UDI
Description: CURAD,PROSORB,ROLLGAUZE,3"X 90", 5CT FDA UDI

Identifiers

Catalog Number: CUR4731435RB FDA UDI
Primary DI / UDI-DI: 00884389159784 FDA UDI
FDA Product Code: NAB FDA UDI
GMDN Term: Orthodontic appliance remover FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4014 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

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

Category: Orthodontic appliance remover

Curad by Medline Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic appliance remover.

Retainer Retriever — STRAIGHT SMILE LLC · Class I
Plasdent — PLASDENT CORP. · Class I
Plasdent — PLASDENT CORP. · Class I
Plasdent — PLASDENT CORP. · Class I
SPECTRUM — ORTHO ARCH COMPANY INC · Class I
SPECTRUM — ORTHO ARCH COMPANY INC · Class I
The Orthodontic Store — Young Innovations, Inc. · Class I
Orthoquest — Young Innovations, Inc. · 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

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

Manufacturer

Manufacturer: Medline Industries, Inc.

Sources (1)

FDA UDI a8981467-69af-4946-b268-f24ee5fd13df 35 fields · synced May 30, 2026