Princeton

FDA UDI

Class I (US FDA UDI)

by Princeton Medical Group, Inc.

Identity

Trade Name: PRINCETON FDA UDI
Generic Name: General-purpose curette FDA UDI
Device Name: EAR CURETTE BUCK STRAIGHT BLUNT 2.7MMØ FIG. 2 FDA UDI
Model / Reference: 45110-02 FDA UDI
Description: EAR CURETTE BUCK STRAIGHT BLUNT 2.7MMØ FIG. 2 FDA UDI

Identifiers

Primary DI / UDI-DI: 00810158217119 FDA UDI
FDA Product Code: FZS FDA UDI
GMDN Term: General-purpose curette 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

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: General-purpose curette

Princeton by Princeton Medical Group, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose curette.

Novo Surgical Inc. — NOVO SURGICAL, INC. · Class I
Dermal Curette — SONTEC INSTRUMENTS, INC. · Class I
Ambler Surgical — Ambler Surgical, LLC · Class I
Curette — Koros USA, Inc. · Class I
BOSS Instruments — Boss Instruments, Ltd. · Class I
Millennium — AVALIGN TECHNOLOGIES, Inc. · Class I
Ambler Surgical — Ambler Surgical, LLC · Class I
Impulse Interbody Spacer System — Degen Medical · 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: Princeton Medical Group, Inc.

Sources (1)

FDA UDI f8f3f198-b8f4-4e33-a90d-699a580fcfa9 33 fields · synced Jun 8, 2026