SAVE 03 (Sinus Curette)

FDA UDI

Class I (US FDA UDI)

by Dentis Co. , Ltd

Identity

Trade Name: SAVE 03 (Sinus Curette) FDA UDI
Generic Name: General-purpose curette FDA UDI
Device Name: Dental Implant Instrument / SAVE 03 (Sinus Curette) FDA UDI
Model / Reference: DSSS03 FDA UDI
Description: Dental Implant Instrument / SAVE 03 (Sinus Curette) FDA UDI

Identifiers

Primary DI / UDI-DI: 08806169145871 FDA UDI
FDA Product Code: NDP FDA UDI
GMDN Term: General-purpose curette FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.3980 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

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: General-purpose curette

SAVE 03 (Sinus Curette) by Dentis Co. , Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose curette.

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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: Dentis Co. , Ltd

Sources (1)

FDA UDI cfdff8b9-3c87-4893-989d-a02371872a6e 33 fields · synced Jun 8, 2026