A. Titan Instruments

FDA UDI

Class I (US FDA UDI)

by A.Titan Instruments

Identity

Trade Name: A. Titan Instruments FDA UDI
Generic Name: Periodontal curette FDA UDI
Device Name: Periodontal Instrument, Curette, Double Ended, Long, HY-LITE Handle FDA UDI
Model / Reference: Gracey 1-2 Long UL FDA UDI
Description: Periodontal Instrument, Curette, Double Ended, Long, HY-LITE Handle FDA UDI

Identifiers

Primary DI / UDI-DI: 00841685106669 FDA UDI
FDA Product Code: EMK FDA UDI
GMDN Term: Periodontal curette 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

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

Dry Heat Sterilization FDA UDI

Category: Periodontal curette

A. Titan Instruments by A.Titan Instruments — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: A.Titan Instruments

Sources (1)

FDA UDI 1d325efe-a8f6-4fa9-8870-0759635673c6 33 fields · synced Jun 9, 2026